An introduction to the GenomicScores package
29 October 2019
Abstract
GenomicScores provides infrastructure to store and access genomewide position-specific scores within R and Bioconductor.Package
GenomicScores 1.10.0
1 Getting started
GenomicScores is an R package distributed as part of the Bioconductor project. To install the package, start R and enter:
install.packages("BiocManager")
BiocManager::install("GenomicScores")Once GenomicScores is installed, it can be loaded with the following command.
library(GenomicScores)Often, however, GenomicScores will be automatically loaded when working with an annotation package that uses GenomicScores, such as phastCons100way.UCSC.hg19.
2 Genomewide position-specific scores
Genomewide scores assign each genomic position a numeric value denoting an estimated measure of constraint or impact on variation at that position. They are commonly used to filter single nucleotide variants or assess the degree of constraint or functionality of genomic features. Genomic scores are built on the basis of different sources of information such as sequence homology, functional domains, physical-chemical changes of amino acid residues, etc.
One particular example of genomic scores are phastCons scores. They provide a measure of conservation obtained from genomewide alignments using the program phast (Phylogenetic Analysis with Space/Time models) from Siepel et al. (2005). The GenomicScores package allows one to retrieve these scores through annotation packages (Section 4) or as AnnotationHub resources (Section 5).
Often, genomic scores such as phastCons are used within workflows running on top of R and Bioconductor. The purpose of the GenomicScores package is to enable an easy and interactive access to genomic scores within those workflows.
3 Lossy storage of genomic scores with compressed vectors
Storing and accessing genomic scores within R is challenging when their values cover large regions of the genome, resulting in gigabytes of double-precision numbers. This is the case, for instance, for phastCons (Siepel et al. 2005), CADD (Kircher et al. 2014) or M-CAP (Jagadeesh et al. 2016) scores.
We address this problem by using lossy compression, also called quantization, coupled with run-length encoding (Rle) vectors. Lossy compression attempts to trade off precision for compression without compromising the scientific integrity of the data (Zender 2016).
Sometimes, measurements and statistical estimates under certain models generate false precision. False precision is essentialy noise that wastes storage space and it is meaningless from the scientific point of view (Zender 2016). In those circumstances, lossy compression not only saves storage space, but also removes false precision.
The use of lossy compression leads to a subset of quantized values much smaller than the original set of genomic scores, resulting in long runs of identical values along the genome. These runs of identical values can be further compressed using the implementation of Rle vectors available in the S4Vectors Bioconductor package.
To enable a seamless access to genomic scores stored with quantized values
in compressed vectors the GenomicScores defines the GScores
class of objects. This class manages the location, loading and dequantization
of genomic scores stored separately on each chromosome.
4 Retrieval of genomic scores through annotation packages
There are currently four different annotation packages that store genomic scores and can be accessed using the GenomicScores package; see Table 1.
| Annotation Package | Description |
|---|---|
| phastCons100way.UCSC.hg19 | phastCons scores derived from the alignment of the human genome (hg19) to other 99 vertebrate species. |
| phastCons100way.UCSC.hg38 | phastCons scores derived from the alignment of the human genome (hg38) to other 99 vertebrate species. |
| phastCons7way.UCSC.hg38 | phastCons scores derived from the alignment of the human genome (hg38) to other 6 mammal species. |
| fitCons.UCSC.hg19 | fitCons scores: fitness consequences of functional annotation for the human genome (hg19). |
This is an example of how genomic scores can be retrieved using the
phastCons100way.UCSC.hg19 package.
Here, a GScores object is created when the package is loaded.
library(phastCons100way.UCSC.hg19)
phast <- phastCons100way.UCSC.hg19
class(phast)## [1] "GScores"
## attr(,"package")
## [1] "GenomicScores"The help page of the GScores class describes the different methods to access the
information and metadata stored in a GScores object. To retrieve genomic scores
for specific positions we should use the function gscores(), as follows.
gscores(phast, GRanges(seqnames="chr22", IRanges(start=50967020:50967025, width=1)))## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020 * | 1
## [2] chr22 50967021 * | 1
## [3] chr22 50967022 * | 0.8
## [4] chr22 50967023 * | 1
## [5] chr22 50967024 * | 1
## [6] chr22 50967025 * | 0
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsThe GenomicScores package only loads the scores data from one sequence to retrieve metadata and from the sequences that are being queried. Note that now the GScores object has loaded the scores from chr22.
phast## GScores object
## # organism: Homo sapiens (UCSC, hg19)
## # provider: UCSC
## # provider version: 09Feb2014
## # download date: Apr 10, 2018
## # loaded sequences: chr19_gl000208_random, chr22
## # number of sites: 2858 millions
## # maximum abs. error: 0.05
## # use 'citation()' to cite these data in publicationsThe bibliographic reference to cite the genomic scores stored in a GScores
object can be accessed using the citation() method either on the package
name or on the GScores object. The latter is implemented in the
GenomicScores package and provides a bibentry object.
citation(phast)## Adam Siepel, Gill Berejano, Jakob S. Pedersen, Angie S. Hinrichs,
## Minmei Hou, Kate Rosenbloom, Hiram Clawson, John Spieth, LaDeana W.
## Hillier, Stephen Richards, George M. Weinstock, Richard K. Wilson,
## Richard A. Gibbs, W. James Kent, Webb Miller, David Haussler (2005).
## "Evolutionarily conserved elements in vertebrate, insect, worm, and
## yeast genomes." _Genome Research_, *15*, 1034-1050. doi:
## 10.1101/gr.3715005 (URL: https://doi.org/10.1101/gr.3715005).Other methods tracing provenance and other metadata are provider(),
providerVersion(), organism() and seqlevelsStyle(); please consult
the help page of the GScores class for a comprehensive list of available
methods.
provider(phast)## [1] "UCSC"providerVersion(phast)## [1] "09Feb2014"organism(phast)## [1] "Homo sapiens"seqlevelsStyle(phast)## [1] "UCSC"5 Retrieval of genomic scores through AnnotationHub resources
Another way to retrieve genomic scores is by using the AnnotationHub, which is a web resource that provides a central location where genomic files (e.g., VCF, bed, wig) and other resources from standard (e.g., UCSC, Ensembl) and distributed sites, can be found. A Bioconductor AnnotationHub web resource creates and manages a local cache of files retrieved by the user, helping with quick and reproducible access.
The first step to retrieve genomic scores is to check the ones available to download.
availableGScores()## [1] "cadd.v1.3.hg19" "fitCons.UCSC.hg19"
## [3] "linsight.UCSC.hg19" "mcap.v1.0.hg19"
## [5] "phastCons7way.UCSC.hg38" "phastCons27way.UCSC.dm6"
## [7] "phastCons46wayPlacental.UCSC.hg19" "phastCons46wayPrimates.UCSC.hg19"
## [9] "phastCons60way.UCSC.mm10" "phastCons100way.UCSC.hg19"
## [11] "phastCons100way.UCSC.hg38" "phyloP60way.UCSC.mm10"
## [13] "phyloP100way.UCSC.hg19" "phyloP100way.UCSC.hg38"The selected resource can be downloaded with the function getGScores(). After the resource is downloaded the first time, the cached copy will enable a quicker retrieval later.
phast <- getGScores("phastCons100way.UCSC.hg19")Finally, the phastCons score of a particular genomic position is retrieved exactly in the same we did with the annotation package.
gscores(phast, GRanges(seqnames="chr22", IRanges(start=50967020:50967025, width=1)))## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020 * | 1
## [2] chr22 50967021 * | 1
## [3] chr22 50967022 * | 0.8
## [4] chr22 50967023 * | 1
## [5] chr22 50967024 * | 1
## [6] chr22 50967025 * | 0
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengths5.1 Building an annotation package from a GScores object
Retrieving genomic scores through AnnotationHub resources requires an internet
connection and we may want to work with such resources offline. For that purpose,
we can create ourselves an annotation package, such as
phastCons100way.UCSC.hg19,
from a GScores object corresponding to a downloaded AnnotationHub resource.
To do that we use the function makeGScoresPackage() as follows:
makeGScoresPackage(phast, maintainer="Me <me@example.com>", author="Me", version="1.0.0")## Creating package in ./phastCons100way.UCSC.hg19An argument, destDir, which by default points to the current working
directory, can be used to change where in the filesystem the package is created.
Afterwards, we should still build and install the package via, e.g.,
R CMD build and R CMD INSTALL, to be able to use it offline.
6 Retrieval of multiple scores per genomic position
Among the score sets available as AnnotationHub web resources shown in the previous section, two of them, CADD (Kircher et al. 2014) and M-CAP (Jagadeesh et al. 2016), provide multiple scores per genomic position that capture the tolerance to mutations of single nucleotides. Using M-CAP scores, we will illustrate how this type of scores are retrieved by default.
mcap <- getGScores("mcap.v1.0.hg19")mcap## GScores object
## # organism: Homo sapiens (UCSC, hg19)
## # provider: Stanford
## # provider version: v1.0
## # download date: Mar 15, 2017
## # loaded sequences: default
## # maximum abs. error: 0.005
## # use 'citation()' to cite these data in publicationscitation(mcap)## Karthik A. Jagadeesh, Aaron M. Wenger, Mark J. Berger, Harendra Guturu,
## Peter D. Stenson, David N. Cooper, Jonathan A. Bernstein, Gill Berejano
## (2016). "M-CAP eliminates a majority of variants of uncertain
## significance in clinical exomes at high sensitivity." _Nature
## Genetics_, *48*, 1581-1586. doi: 10.1038/ng.3703 (URL:
## https://doi.org/10.1038/ng.3703).gr <- GRanges(seqnames="chr22", IRanges(50967020:50967025, width=1))
gscores(mcap, gr)## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <matrix>
## [1] chr22 50967020 * | 0.54:0.55:0.34
## [2] chr22 50967021 * | 0.47:0.64:0.64
## [3] chr22 50967022 * | NA:NA:NA
## [4] chr22 50967023 * | 0.57:0.39:0.46
## [5] chr22 50967024 * | NA:0.5:0.49
## [6] chr22 50967025 * | NA:0.59:0.59
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsThe previous call to the gscores() method returns three scores per position
corresponding to the M-CAP scores that estimate the tolerance of mutating the
reference nucleotide at that position to each of the possible alternative
alleles, in alphabetical order. One may directly retrieve the scores for
combinations of reference and alternative alelles using the ref and alt
arguments of the gscores() method. See the following example with the
the previous genomic positions and some randomly selected alternative alleles.
library(BSgenome.Hsapiens.UCSC.hg19)
refAlleles <- as.character(getSeq(Hsapiens, gr))
altAlleles <- DNA_BASES[(match(refAlleles, DNA_BASES)) %% 4 + 1]
cbind(REF=refAlleles, ALT=altAlleles)## REF ALT
## [1,] "C" "G"
## [2,] "G" "T"
## [3,] "T" "A"
## [4,] "C" "G"
## [5,] "C" "G"
## [6,] "G" "T"gscores(mcap, gr, ref=refAlleles, alt=altAlleles)## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020 * | 0.55
## [2] chr22 50967021 * | 0.64
## [3] chr22 50967022 * | <NA>
## [4] chr22 50967023 * | 0.39
## [5] chr22 50967024 * | 0.5
## [6] chr22 50967025 * | 0.59
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengths7 Summarization of genomic scores
The input genomic ranges to the gscores() method may have widths larger than one
nucleotide. In those cases, and when there is only one score per position, the
gscores() method calculates, by default, the arithmetic mean of the scores across
each range.
gr1 <- GRanges(seqnames="chr22", IRanges(start=50967020:50967025, width=1))
gr1sco <- gscores(phast, gr1)
gr1sco## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020 * | 1
## [2] chr22 50967021 * | 1
## [3] chr22 50967022 * | 0.8
## [4] chr22 50967023 * | 1
## [5] chr22 50967024 * | 1
## [6] chr22 50967025 * | 0
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsmean(gr1sco$default)## [1] 0.8gr2 <- GRanges("chr22:50967020-50967025")
gscores(phast, gr2)## GRanges object with 1 range and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020-50967025 * | 0.8
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsHowever, we may change the way in which scores from multiple-nucleotide ranges are
summarized with the argument summaryFun, as follows.
gscores(phast, gr2, summaryFun=max)## GRanges object with 1 range and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020-50967025 * | 1
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsgscores(phast, gr2, summaryFun=min)## GRanges object with 1 range and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020-50967025 * | 0
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsgscores(phast, gr2, summaryFun=median)## GRanges object with 1 range and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020-50967025 * | 1
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengths8 Retrieval of quantized genomic scores
The specific quantization and dequantization functions are stored as part of
the metadata of a GScores object and they can be examined with the methods
qfun() and dqfun(), respectively. The latter is called by the gscores()
method to retrieve genomic scores.
phastqfun <- qfun(phast)
phastqfun## function (x)
## {
## q <- as.integer(sprintf("%.0f", 10 * x))
## q <- q + 1L
## q
## }
## attr(,"description")
## [1] "multiply by 10, round to nearest integer, add up one"phastdqfun <- dqfun(phast)
phastdqfun## function (q)
## {
## x <- as.numeric(q)
## x[x == 0] <- NA
## x <- (x - 1)/10
## x
## }
## <bytecode: 0x558f783ea0f0>
## attr(,"description")
## [1] "subtract one integer unit, divide by 10"For single-nucleotide ranges, we can retrieve the quantized genomic scores
using the argument quantized=TRUE.
gr1sco <- gscores(phast, gr1, quantized=TRUE)
gr1sco## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | default
## <Rle> <IRanges> <Rle> | <Rle>
## [1] chr22 50967020 * | 0b
## [2] chr22 50967021 * | 0b
## [3] chr22 50967022 * | 09
## [4] chr22 50967023 * | 0b
## [5] chr22 50967024 * | 0b
## [6] chr22 50967025 * | 01
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsUsing the dequantization function we can obtain later the genomic scores.
phastdqfun(gr1sco$default)## [1] 1.0 1.0 0.8 1.0 1.0 0.09 Populations of scores
A single GScores object may store multiple populations of scores of the same
kind. One such case is when scores are stored with different precision levels.
This is the case for the package phastCons100way.UCSC.hg19, in
which phastCons scores are compressed rounding values to 1 and 2 decimal
places. To figure out what are the available score populations in a GScores
object we should use the method populations():
populations(phast)## [1] "default" "DP2"Whenever one of these populations is called default, this is the one used
by default. In other cases we can find out which is the default population as
follows:
defaultPopulation(phast)## [1] "default"To use one of the available score populations we should use the argument
pop in the corresponding methods, as follows:
gscores(phast, gr1, pop="DP2")## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | DP2
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020 * | 0.98
## [2] chr22 50967021 * | 0.98
## [3] chr22 50967022 * | 0.83
## [4] chr22 50967023 * | 0.99
## [5] chr22 50967024 * | 0.96
## [6] chr22 50967025 * | 0
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsqfun(phast, pop="DP2")## function (x)
## {
## q <- as.integer(sprintf("%.0f", 100 * x))
## q <- q + 1L
## q
## }
## attr(,"description")
## [1] "multiply by 100, round to nearest integer, add up one"dqfun(phast, pop="DP2")## function (q)
## {
## x <- as.numeric(q)
## x[x == 0] <- NA
## x <- (x - 1)/100
## x
## }
## attr(,"description")
## [1] "subtract one integer unit, divide by 100"We can also change the default scores population to use, as follows:
defaultPopulation(phast) <- "DP2"
phast## GScores object
## # organism: Homo sapiens (UCSC, hg19)
## # provider: UCSC
## # provider version: 09Feb2014
## # download date: Apr 10, 2018
## # loaded sequences: chr19_gl000208_random, chr22
## # loaded populations: default, DP2
## # default scores population: DP2
## # number of sites: 2858 millions
## # maximum abs. error (def. pop.): 0.005
## # use 'citation()' to cite these data in publicationsgscores(phast, gr1)## GRanges object with 6 ranges and 1 metadata column:
## seqnames ranges strand | DP2
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr22 50967020 * | 0.98
## [2] chr22 50967021 * | 0.98
## [3] chr22 50967022 * | 0.83
## [4] chr22 50967023 * | 0.99
## [5] chr22 50967024 * | 0.96
## [6] chr22 50967025 * | 0
## -------
## seqinfo: 1 sequence from Genome Reference Consortium GRCh37 genome; no seqlengthsqfun(phast)## function (x)
## {
## q <- as.integer(sprintf("%.0f", 100 * x))
## q <- q + 1L
## q
## }
## attr(,"description")
## [1] "multiply by 100, round to nearest integer, add up one"dqfun(phast)## function (q)
## {
## x <- as.numeric(q)
## x[x == 0] <- NA
## x <- (x - 1)/100
## x
## }
## <bytecode: 0x558f76e3cf20>
## attr(,"description")
## [1] "subtract one integer unit, divide by 100"10 Retrieval of minor allele frequency data
One particular type of genomic scores that are accessible through
the GScores class is minor allele frequency (MAF) data.
There are currently 17 annotation packages that store MAF values
using the GenomicScores package, named using the
prefix MafDb; see Table 2 below.
| Annotation Package | Description |
|---|---|
| MafDb.1Kgenomes.phase1.hs37d5 | MAF data from the 1000 Genomes Project Phase 1 for the human genome version GRCh37. |
| MafDb.1Kgenomes.phase1.GRCh38 | MAF data from the 1000 Genomes Project Phase 1 for the human genome version GRCh38. |
| MafDb.1Kgenomes.phase3.hs37d5 | MAF data from the 1000 Genomes Project Phase 3 for the human genome version GRCh37. |
| MafDb.1Kgenomes.phase3.GRCh38 | MAF data from the 1000 Genomes Project Phase 3 for the human genome version GRCh38. |
| MafDb.ESP6500SI.V2.SSA137.hs37d5 | MAF data from NHLBI ESP 6500 exomes for the human genome version GRCh37. |
| MafDb.ESP6500SI.V2.SSA137.GRCh38 | MAF data from NHLBI ESP 6500 exomes for the human genome version GRCh38. |
| MafDb.ExAC.r1.0.hs37d5 | MAF data from ExAC 60706 exomes for the human genome version GRCh37. |
| MafDb.ExAC.r1.0.GRCh38 | MAF data from ExAC 60706 exomes for the human genome version GRCh38. |
| MafDb.ExAC.r1.0.nonTCGA.hs37d5 | MAF data from ExAC 53105 nonTCGA exomes for the human genome version GRCh37. |
| MafDb.ExAC.r1.0.nonTCGA.GRCh38 | MAF data from ExAC 53105 nonTCGA exomes for the human genome version GRCh38. |
| MafDb.gnomAD.r2.1.hs37d5 | MAF data from gnomAD 15496 genomes for the human genome version GRCh37. |
| MafDb.gnomAD.r2.1.GRCh38 | MAF data from gnomAD 15496 genomes for the human genome version GRCh38. |
| MafDb.gnomADex.r2.1.hs37d5 | MAF data from gnomADex 123136 exomes for the human genome version GRCh37. |
| MafDb.gnomADex.r2.1.GRCh38 | MAF data from gnomADex 123136 exomes for the human genome version GRCh38. |
| MafDb.gnomAD.r3.0.GRCh38 | MAF data from gnomAD 71702 genomes for the human genome version GRCh38. |
| MafDb.TOPMed.freeze5.hg19 | MAF data from NHLBI TOPMed 62784 genomes for the human genome version GRCh37. |
| MafDb.TOPMed.freeze5.hg38 | MAF data from NHLBI TOPMed 62784 genomes for the human genome version GRCh38. |
In this context, the scores populations correspond to populations of individuals from which the MAF data were derived, while all MAF data were compressed using a precision of one significant figure for MAF < 0.1 and two significant figures for MAF >= 0.1.
library(MafDb.1Kgenomes.phase1.hs37d5)
mafdb <- MafDb.1Kgenomes.phase1.hs37d5
mafdb## GScores object
## # organism: Homo sapiens (1000genomes, hs37d5)
## # provider: IGSR
## # provider version: Phase1
## # download date: Oct 23, 2019
## # loaded sequences (SNRs): 22
## # loaded sequences (nonSNRs): none
## # default scores population: AF
## # number of sites: 40 millions
## # maximum abs. error (def. pop.): 0.000141
## # use 'citation()' to cite these data in publicationspopulations(mafdb)## [1] "AF" "AFR_AF" "AMR_AF" "ASN_AF" "EUR_AF"Consider the following example in which we are interested in MAF values for variants associated with eye color. We can start by fetching the corresponding variant identifers from the GWAS catalog using the gwascat package, as follows.
library(gwascat)
data(ebicat37)
eyersids <- unique(subsetByTraits(ebicat37, tr="Eye color")$SNPS)
eyersids## [1] "rs12913832" "rs7173419" "rs3002288" "rs12896399" "rs1408799"
## [6] "rs12520016" "rs288139" "rs1667394" "rs4596632" "rs12203592"
## [11] "rs16891982" "rs1393350" "rs1847134"We query the genomic position of the variant identifier through the SNPlocs.Hsapiens.dbSNP144.GRCh37 package, which stores the build 144 of the dbSNP database.
library(SNPlocs.Hsapiens.dbSNP144.GRCh37)
rng <- snpsById(SNPlocs.Hsapiens.dbSNP144.GRCh37, ids=eyersids)
rng## UnstitchedGPos object with 13 positions and 2 metadata columns:
## seqnames pos strand | RefSNP_id alleles_as_ambig
## <Rle> <integer> <Rle> | <character> <character>
## [1] 15 28365618 * | rs12913832 R
## [2] 15 28196821 * | rs7173419 Y
## [3] 1 213126565 * | rs3002288 R
## [4] 14 92773663 * | rs12896399 K
## [5] 9 12672097 * | rs1408799 Y
## ... ... ... ... . ... ...
## [9] 8 132353735 * | rs4596632 R
## [10] 6 396321 * | rs12203592 Y
## [11] 5 33951693 * | rs16891982 S
## [12] 11 89011046 * | rs1393350 R
## [13] 11 89005253 * | rs1847134 M
## -------
## seqinfo: 25 sequences (1 circular) from GRCh37.p13 genomeFinally, fetch the MAF values on those positions.
eyecolormafs <- gscores(mafdb, rng, pop=c("AF", "EUR_AF", "AFR_AF"))## assuming GRCh37.p13 and hs37d5 represent the same genome build between query ranges and the GScores object, respectively.eyecolormafs## UnstitchedGPos object with 13 positions and 5 metadata columns:
## seqnames pos strand | RefSNP_id alleles_as_ambig AF
## <Rle> <integer> <Rle> | <character> <character> <numeric>
## [1] 15 28365618 * | rs12913832 R 0.29
## [2] 15 28196821 * | rs7173419 Y 0.44
## [3] 1 213126565 * | rs3002288 R 0.33
## [4] 14 92773663 * | rs12896399 K 0.29
## [5] 9 12672097 * | rs1408799 Y 0.35
## ... ... ... ... . ... ... ...
## [9] 8 132353735 * | rs4596632 R 0.45
## [10] 6 396321 * | rs12203592 Y 0.05
## [11] 5 33951693 * | rs16891982 S 0.44
## [12] 11 89011046 * | rs1393350 R 0.11
## [13] 11 89005253 * | rs1847134 M 0.22
## EUR_AF AFR_AF
## <numeric> <numeric>
## [1] 0.29 0.04
## [2] 0.25 0.26
## [3] 0.46 0.08
## [4] 0.43 0.03
## [5] 0.34 0.22
## ... ... ...
## [9] 0.32 0.46
## [10] 0.11 0.01
## [11] 0.03 0.05
## [12] 0.24 0.01
## [13] 0.3 0.15
## -------
## seqinfo: 25 sequences (1 circular) from hs37d5 genomeSometimes, data producers may annotate identifiers to genomic scores, such as dbSNP rs identifiers to MAF values. In such a case, we can directly attempt to fetch genomic scores using those identifiers as follows.
gscores(mafdb, eyersids, pop=c("AF", "EUR_AF", "AFR_AF"))## Loading first time annotations of identifiers to genomic positions, produced by data provider.## GRanges object with 13 ranges and 3 metadata columns:
## seqnames ranges strand | AF EUR_AF AFR_AF
## <Rle> <IRanges> <Rle> | <numeric> <numeric> <numeric>
## rs12913832 15 28365618 * | 0.29 0.29 0.04
## rs7173419 15 28196821 * | 0.44 0.25 0.26
## rs3002288 1 213126565 * | 0.33 0.46 0.08
## rs12896399 14 92773663 * | 0.29 0.43 0.03
## rs1408799 9 12672097 * | 0.35 0.34 0.22
## ... ... ... ... . ... ... ...
## rs4596632 8 132353735 * | 0.45 0.32 0.46
## rs12203592 6 396321 * | 0.05 0.11 0.01
## rs16891982 5 33951693 * | 0.44 0.03 0.05
## rs1393350 11 89011046 * | 0.11 0.24 0.01
## rs1847134 11 89005253 * | 0.22 0.3 0.15
## -------
## seqinfo: 23 sequences from hs37d5 genome; no seqlengthsThe following code produces the barplot shown in Figure 1 illustrating graphically the differences in MAF values from these variants between the three queried populations.
par(mar=c(3, 5, 1, 1))
mafpops <- c("AF", "EUR_AF", "AFR_AF")
bp <- barplot(t(as.matrix(mcols(eyecolormafs)[, mafpops])), beside=TRUE,
col=c("darkblue", "darkgreen", "darkorange"),
ylim=c(0, 0.55), las=1, ylab="Minor allele frequency")
axis(1, bp[2, ], 1:length(eyecolormafs))
mtext("Variant", side=1, line=2)
legend("topright", mafpops, fill=c("darkblue", "darkgreen", "darkorange"))
Figure 1: Eye color MAFs
Minor allele frequencies (MAFs) of variants associated with eye color for global, european and african populations of the Phase 1 data from the 1000 Genomes Project.
11 Annotating variants with genomic scores
A typical use case of the GenomicScores package is in the context of annotating variants with genomic scores, such as phastCons conservation scores. For this purpose, we load the VariantAnnotaiton and TxDb.Hsapiens.UCSC.hg19.knownGene packages. The former will allow us to read a VCF file and annotate it, and the latter contains the gene annotations from UCSC that will be used in this process.
library(VariantAnnotation)
library(TxDb.Hsapiens.UCSC.hg19.knownGene)Let’s load one of the sample VCF files that form part of the VariantAnnotation package.
fl <- system.file("extdata", "chr22.vcf.gz", package="VariantAnnotation")
vcf <- readVcf(fl, "hg19")
seqlevelsStyle(vcf)## [1] "NCBI" "Ensembl"txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene
seqlevelsStyle(txdb)## [1] "UCSC"Because the chromosome nomenclature from the VCF file (NCBI) is different
from the one with the gene annotations (UCSC) we use the seqlevelsStyle()
function to force our variants having the chromosome nomenclature of the
gene annotations.
seqlevelsStyle(vcf) <- seqlevelsStyle(txdb)We annotate the location of variants using the function locateVariants()
from the VariantAnnotation package.
loc <- locateVariants(vcf, txdb, AllVariants())## Warning in valid.GenomicRanges.seqinfo(x, suggest.trim = TRUE): GRanges object contains 2405 out-of-bound ranges located on sequences
## 75253, 74357, 74359, 74360, 74361, 74362, 74363, 74358, 74364, 74365,
## 75254, 75259, 74368, 74369, 74366, 74367, 74370, 74372, 74373, 74374,
## 74375, 74378, 74377, 74380, 74381, 75262, 75263, 75265, 75266, 75268,
## 75269, 75271, 75273, 75276, 75281, 75282, 75283, 74389, 74383, 74384,
## 74385, 74386, 74387, 75287, 75288, 75286, 75289, 74390, 74391, 74392,
## 74393, 74394, 75291, 74395, 74396, 74397, 74398, 75302, 75304, 75305,
## and 75306. Note that ranges located on a sequence whose length is
## unknown (NA) or on a circular sequence are not considered out-of-bound
## (use seqlengths() and isCircular() to get the lengths and circularity
## flags of the underlying sequences). You can use trim() to trim these
## ranges. See ?`trim,GenomicRanges-method` for more information.loc[1:3]## GRanges object with 3 ranges and 9 metadata columns:
## seqnames ranges strand | LOCATION LOCSTART LOCEND
## <Rle> <IRanges> <Rle> | <factor> <integer> <integer>
## rs7410291 chr22 50300078 - | intron 10763 10763
## rs147922003 chr22 50300086 - | intron 10755 10755
## rs114143073 chr22 50300101 - | intron 10740 10740
## QUERYID TXID CDSID GENEID PRECEDEID
## <integer> <character> <IntegerList> <character> <CharacterList>
## rs7410291 1 75253 <NA> 79087 <NA>
## rs147922003 2 75253 <NA> 79087 <NA>
## rs114143073 3 75253 <NA> 79087 <NA>
## FOLLOWID
## <CharacterList>
## rs7410291 <NA>
## rs147922003 <NA>
## rs114143073 <NA>
## -------
## seqinfo: 1 sequence from hg19 genome; no seqlengthstable(loc$LOCATION)##
## spliceSite intron fiveUTR threeUTR coding intergenic promoter
## 11 22572 309 1368 2822 2867 2864Annotate phastCons conservation scores on the variants and store
those annotations as an additional metadata column of the GRanges object.
For this specific purpose we should use the method score() that returns
the genomic scores as a numeric vector instead as a metadata column in the
input ranges object.
loc$PHASTCONS <- score(phast, loc)## assuming hg19 and Genome Reference Consortium GRCh37 represent the same genome build between query ranges and the GScores object, respectively.loc[1:3]## GRanges object with 3 ranges and 10 metadata columns:
## seqnames ranges strand | LOCATION LOCSTART LOCEND
## <Rle> <IRanges> <Rle> | <factor> <integer> <integer>
## rs7410291 chr22 50300078 - | intron 10763 10763
## rs147922003 chr22 50300086 - | intron 10755 10755
## rs114143073 chr22 50300101 - | intron 10740 10740
## QUERYID TXID CDSID GENEID PRECEDEID
## <integer> <character> <IntegerList> <character> <CharacterList>
## rs7410291 1 75253 <NA> 79087 <NA>
## rs147922003 2 75253 <NA> 79087 <NA>
## rs114143073 3 75253 <NA> 79087 <NA>
## FOLLOWID PHASTCONS
## <CharacterList> <numeric>
## rs7410291 <NA> 0
## rs147922003 <NA> 0.08
## rs114143073 <NA> 0
## -------
## seqinfo: 1 sequence from hg19 genome; no seqlengthsUsing the following code we can examine the distribution of phastCons conservation scores of variants across the different annotated regions, shown in Figure 2.
x <- split(loc$PHASTCONS, loc$LOCATION)
mask <- elementNROWS(x) > 0
boxplot(x[mask], ylab="phastCons score", las=1, cex.axis=1.2, cex.lab=1.5, col="gray")
points(1:length(x[mask])+0.25, sapply(x[mask], mean, na.rm=TRUE), pch=23, bg="black")
Figure 2: Distribution of phastCons conservation scores in variants across different annotated regions
Diamonds indicate mean values.
Next, we can annotate M-CAP and CADD scores as follows. Note that we need to take
care to only query positions of single nucleotide variants, and using the QUERYID
column of the annotations to fetch back reference and alternative alleles from the
original VCF file container.
maskSNVs <- isSNV(vcf)[loc$QUERYID]
loc$MCAP <- rep(NA_real_, length(loc))
loc$MCAP[maskSNVs] <- score(mcap, loc[maskSNVs],
ref=ref(vcf)[loc$QUERYID[maskSNVs]],
alt=alt(vcf)[loc$QUERYID[maskSNVs]])## assuming hg19 and Genome Reference Consortium GRCh37 represent the same genome build between query ranges and the GScores object, respectively.maskSNVs <- isSNV(vcf)[loc$QUERYID]
loc$CADD <- rep(NA_real_, length(loc))
loc$CADD[maskSNVs] <- score(cadd, loc[maskSNVs],
ref=ref(vcf)[loc$QUERYID[maskSNVs]],
alt=alt(vcf)[loc$QUERYID[maskSNVs]])## assuming hg19 and Genome Reference Consortium GRCh37 represent the same genome build between query ranges and the GScores object, respectively.Using the code below we can produce the plot of Figure 3 comparing CADD and M-CAP scores and labeling the location of the variants from which they are derived.
library(RColorBrewer)
par(mar=c(4, 5, 1, 1))
hmcol <- colorRampPalette(brewer.pal(nlevels(loc$LOCATION), "Set1"))(nlevels(loc$LOCATION))
plot(jitter(loc$MCAP, factor=2), jitter(loc$CADD, factor=2), pch=19,
col=hmcol, xlab="M-CAP scores", ylab="CADD scores",
las=1, cex.axis=1.2, cex.lab=1.5, panel.first=grid())
legend("bottomright", levels(loc$LOCATION), pch=19, col=hmcol, inset=0.01)
Figure 3: Comparison of M-CAP and CADD scores
Values on the x- and y-axis are jittered to facilitate visualization.
Finally, we will show how to annotate MAF values on these variants. However,
in this particular case, we should take care of the different sequence styles
(UCSC vs NCBI) and genome version nomenclatures (hg19 vs. hs37d5) between the
annotated variants and the GScores object.
seqlevelsStyle(loc) <- seqlevelsStyle(mafdb)[1]
seqinfo(loc, new2old=match(seqlevels(mafdb), seqlevels(loc))) <- seqinfo(mafdb)
maskSNVs <- isSNV(vcf)[loc$QUERYID]
loc$MAF[maskSNVs] <- gscores(mafdb, loc[maskSNVs])$AF
loc$MAF[!maskSNVs] <- gscores(mafdb, loc[!maskSNVs], type="nonsnrs")$AF
loc[1:3]## GRanges object with 3 ranges and 13 metadata columns:
## seqnames ranges strand | LOCATION LOCSTART LOCEND
## <Rle> <IRanges> <Rle> | <factor> <integer> <integer>
## rs7410291 22 50300078 - | intron 10763 10763
## rs147922003 22 50300086 - | intron 10755 10755
## rs114143073 22 50300101 - | intron 10740 10740
## QUERYID TXID CDSID GENEID PRECEDEID
## <integer> <character> <IntegerList> <character> <CharacterList>
## rs7410291 1 75253 <NA> 79087 <NA>
## rs147922003 2 75253 <NA> 79087 <NA>
## rs114143073 3 75253 <NA> 79087 <NA>
## FOLLOWID PHASTCONS MCAP CADD MAF
## <CharacterList> <numeric> <numeric> <numeric> <numeric>
## rs7410291 <NA> 0 <NA> 0 0.34
## rs147922003 <NA> 0.08 <NA> 10 0.01
## rs114143073 <NA> 0 <NA> 0 0.01
## -------
## seqinfo: 86 sequences (1 circular) from hs37d5 genomeWe also show that by providing reference and alternate alleles through
the arguments ref and alt, we can obtain their individual allele
frequencies. The current lossy compression of these values yields their
correct asignment in the case of biallelic variants and an aproximation
in the case of multiallelic ones.
afs <- DataFrame(matrix(NA, nrow=length(loc), ncol=2,
dimnames=list(NULL, c("AF_REF", "AF_ALT"))))
afs[maskSNVs, ] <- score(mafdb, loc[maskSNVs],
ref=ref(vcf)[loc$QUERYID[maskSNVs]],
alt=alt(vcf)[loc$QUERYID[maskSNVs]])
afs[!maskSNVs, ] <- score(mafdb, loc[!maskSNVs],
ref=ref(vcf)[loc$QUERYID[!maskSNVs]],
alt=alt(vcf)[loc$QUERYID[!maskSNVs]],
type="nonsnrs")
mcols(loc) <- cbind(mcols(loc), afs)
loc[1:3]## GRanges object with 3 ranges and 15 metadata columns:
## seqnames ranges strand | LOCATION LOCSTART LOCEND
## <Rle> <IRanges> <Rle> | <factor> <integer> <integer>
## rs7410291 22 50300078 - | intron 10763 10763
## rs147922003 22 50300086 - | intron 10755 10755
## rs114143073 22 50300101 - | intron 10740 10740
## QUERYID TXID CDSID GENEID PRECEDEID
## <integer> <character> <IntegerList> <character> <CharacterList>
## rs7410291 1 75253 <NA> 79087 <NA>
## rs147922003 2 75253 <NA> 79087 <NA>
## rs114143073 3 75253 <NA> 79087 <NA>
## FOLLOWID PHASTCONS MCAP CADD MAF AF_REF
## <CharacterList> <numeric> <numeric> <numeric> <numeric> <numeric>
## rs7410291 <NA> 0 <NA> 0 0.34 0.66
## rs147922003 <NA> 0.08 <NA> 10 0.01 0.99
## rs114143073 <NA> 0 <NA> 0 0.01 0.99
## AF_ALT
## <numeric>
## rs7410291 0.34
## rs147922003 0.01
## rs114143073 0.01
## -------
## seqinfo: 86 sequences (1 circular) from hs37d5 genome12 Comparison between lossy-compressed and original phastCons scores
To have a sense of the extent of the trade-off between precision and compression in a specific case,
we compare here original phastCons scores with the ones obtained by rounding their precision to
one significant figure, and stored in the annotation package phastCons100way.UCSC.hg19.
Because phastCons scores measure conservation, we sampled uniformly at random one
thousand phastCons scores from differently conserved regions, concretely CDS and 3’UTR.
These sampled scores are included in this package to illustrate this comparison.
Interestingly, among the phastCons scores sampled from 1000 CDS positions,
there are only 198 different values despite the apparently very high precision of some of them.
origpcscoCDS <- readRDS(system.file("extdata", "origphastCons100wayhg19CDS.rds", package="GenomicScores"))
origpcscoCDS## GRanges object with 1000 ranges and 1 metadata column:
## seqnames ranges strand | score
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr1 976248 * | 0.763999998569489
## [2] chr1 1886625 * | 0.00300000002607703
## [3] chr1 3751636 * | 1
## [4] chr1 5950945 * | 0.236000001430511
## [5] chr1 6638784 * | 0.99099999666214
## ... ... ... ... . ...
## [996] chrX 154113587 * | 1
## [997] chrX 154261706 * | 1
## [998] chrX 154305499 * | 1
## [999] chrY 15481226 * | 1
## [1000] chrY 21871402 * | 0.981000006198883
## -------
## seqinfo: 25 sequences from an unspecified genomelength(unique(origpcscoCDS$score))## [1] 198We look more closely the number of significant figures of precision used in these original phastCons scores.
numDecimals <- function(x) {
spl <- strsplit(as.character(x+1), "\\.")
spl <- sapply(spl, "[", 2)
spl[is.na(spl)] <- ""
nchar(spl)
}
nd1 <- numDecimals(origpcscoCDS$score)
table(nd1)## nd1
## 0 1 2 12 13 14
## 637 1 2 5 63 292Similarly, in 3’UTR regions, only 209 unique phastCons scores are observed.
origpcsco3UTRs <- readRDS(system.file("extdata", "origphastCons100wayhg193UTR.rds", package="GenomicScores"))
origpcsco3UTRs## GRanges object with 1000 ranges and 1 metadata column:
## seqnames ranges strand | score
## <Rle> <IRanges> <Rle> | <numeric>
## [1] chr1 1189930 * | 0
## [2] chr1 1227810 * | 0
## [3] chr1 1595390 * | 0.0149999996647239
## [4] chr1 1595685 * | 0
## [5] chr1 2336044 * | 0
## ... ... ... ... . ...
## [996] chrX 125684491 * | 0
## [997] chrX 129190576 * | 1
## [998] chrX 135299066 * | 0.196999996900558
## [999] chrX 148560948 * | 0.00300000002607703
## [1000] chrX 153289202 * | 0
## -------
## seqinfo: 25 sequences from an unspecified genomelength(table(origpcsco3UTRs$score))## [1] 209nd2 <- numDecimals(origpcsco3UTRs$score)
table(nd2)## nd2
## 0 12 13 14
## 502 3 112 383Reset the default scores population to the one that achieves more compression by rounding to 1 decimal place.
defaultPopulation(phast) <- "default"
phast## GScores object
## # organism: Homo sapiens (UCSC, hg19)
## # provider: UCSC
## # provider version: 09Feb2014
## # download date: Apr 10, 2018
## # loaded sequences: chr19_gl000208_random, chr22
## # loaded populations: default, DP2
## # number of sites: 2858 millions
## # maximum abs. error: 0.05
## # use 'citation()' to cite these data in publicationsRetrieve the corresponding phastCons scores stored in the annotation package.
pkgpcscoCDS <- score(phast, origpcscoCDS)
pkgpcsco3UTRs <- score(phast, origpcsco3UTRs)In Figure 4 we show a visual comparison between raw and rounded phastCons scores. The two panels on top compare the whole range of scores observed in CDS (left) and 3’UTR (right) regions. However, the rounding effect can be better observed in the cumulative distributions shown in the panels at the bottom, again for CDS (left) and 3’UTR (right) regions.
In these bottom panels, phastcons scores in CDS and 3’UTR regions display very different cumulative distributions. In CDS regions, most of the genomic scores (>60%) are found between the values of 0.9 and 1.0, while around 25% of the scores are found below 0.1. Indeed, these are the range of values where lossy compression loses more precison. The cumulative distribution of 3’UTR shows the same critical points, with the difference that most of scores are found below 0.1 (>70%).
Figure 4: Original and lossy-compressed phastCons scores
Top panels (a, b): comparison of the distribution of values. Bottom panels (c, d): comparison of the cumulative distribution
The bottom plots in Figure 4 also reveal that when the cumulative distribution is of interest, such as in the context of filtering genetic variants above or below certain threshold of conservation, the quantization of phastCons scores to 1 decimal place provides sufficient precision for a wide range of conservation values.
13 Session information
sessionInfo()## R version 3.6.1 (2019-07-05)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 18.04.3 LTS
##
## Matrix products: default
## BLAS: /home/biocbuild/bbs-3.10-bioc/R/lib/libRblas.so
## LAPACK: /home/biocbuild/bbs-3.10-bioc/R/lib/libRlapack.so
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=C
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## attached base packages:
## [1] parallel stats4 stats graphics grDevices utils datasets
## [8] methods base
##
## other attached packages:
## [1] RColorBrewer_1.1-2
## [2] VariantAnnotation_1.32.0
## [3] Rsamtools_2.2.0
## [4] SummarizedExperiment_1.16.0
## [5] DelayedArray_0.12.0
## [6] BiocParallel_1.20.0
## [7] matrixStats_0.55.0
## [8] SNPlocs.Hsapiens.dbSNP144.GRCh37_0.99.20
## [9] gwascat_2.18.0
## [10] Homo.sapiens_1.3.1
## [11] TxDb.Hsapiens.UCSC.hg19.knownGene_3.2.2
## [12] org.Hs.eg.db_3.10.0
## [13] GO.db_3.10.0
## [14] OrganismDbi_1.28.0
## [15] GenomicFeatures_1.38.0
## [16] AnnotationDbi_1.48.0
## [17] Biobase_2.46.0
## [18] MafDb.1Kgenomes.phase1.hs37d5_3.10.0
## [19] BSgenome.Hsapiens.UCSC.hg19_1.4.0
## [20] BSgenome_1.54.0
## [21] rtracklayer_1.46.0
## [22] Biostrings_2.54.0
## [23] XVector_0.26.0
## [24] phastCons100way.UCSC.hg19_3.7.2
## [25] GenomicScores_1.10.0
## [26] GenomicRanges_1.38.0
## [27] GenomeInfoDb_1.22.0
## [28] IRanges_2.20.0
## [29] S4Vectors_0.24.0
## [30] BiocGenerics_0.32.0
## [31] BiocStyle_2.14.0
##
## loaded via a namespace (and not attached):
## [1] httr_1.4.1 bit64_0.9-7
## [3] AnnotationHub_2.18.0 shiny_1.4.0
## [5] assertthat_0.2.1 askpass_1.1
## [7] interactiveDisplayBase_1.24.0 highr_0.8
## [9] BiocManager_1.30.9 BiocFileCache_1.10.0
## [11] RBGL_1.62.0 blob_1.2.0
## [13] GenomeInfoDbData_1.2.2 yaml_2.2.0
## [15] progress_1.2.2 BiocVersion_3.10.1
## [17] pillar_1.4.2 RSQLite_2.1.2
## [19] backports_1.1.5 lattice_0.20-38
## [21] glue_1.3.1 digest_0.6.22
## [23] promises_1.1.0 htmltools_0.4.0
## [25] httpuv_1.5.2 Matrix_1.2-17
## [27] XML_3.98-1.20 pkgconfig_2.0.3
## [29] biomaRt_2.42.0 bookdown_0.14
## [31] zlibbioc_1.32.0 purrr_0.3.3
## [33] xtable_1.8-4 later_1.0.0
## [35] openssl_1.4.1 tibble_2.1.3
## [37] magrittr_1.5 crayon_1.3.4
## [39] mime_0.7 memoise_1.1.0
## [41] evaluate_0.14 graph_1.64.0
## [43] prettyunits_1.0.2 tools_3.6.1
## [45] hms_0.5.1 stringr_1.4.0
## [47] compiler_3.6.1 rlang_0.4.1
## [49] grid_3.6.1 RCurl_1.95-4.12
## [51] rappdirs_0.3.1 bitops_1.0-6
## [53] rmarkdown_1.16 DBI_1.0.0
## [55] curl_4.2 R6_2.4.0
## [57] GenomicAlignments_1.22.0 knitr_1.25
## [59] dplyr_0.8.3 fastmap_1.0.1
## [61] bit_1.1-14 zeallot_0.1.0
## [63] stringi_1.4.3 Rcpp_1.0.2
## [65] vctrs_0.2.0 dbplyr_1.4.2
## [67] tidyselect_0.2.5 xfun_0.10References
Jagadeesh, Karthik A, Aaron M Wenger, Mark J Berger, Harendra Guturu, Peter D Stenson, David N Cooper, Jonathan A Bernstein, and Gill Bejerano. 2016. “M-Cap Eliminates a Majority of Variants of Uncertain Significance in Clinical Exomes at High Sensitivity.” Nat. Genet. 48 (12). Nature Publishing Group:1581–6.
Kircher, Martin, Daniela M Witten, Preti Jain, Brian J O’roak, Gregory M Cooper, and Jay Shendure. 2014. “A General Framework for Estimating the Relative Pathogenicity of Human Genetic Variants.” Nat. Genet. 46 (3). Nature Publishing Group:310–15.
Siepel, Adam, Gill Bejerano, Jakob S Pedersen, Angie S Hinrichs, Minmei Hou, Kate Rosenbloom, Hiram Clawson, et al. 2005. “Evolutionarily Conserved Elements in Vertebrate, Insect, Worm, and Yeast Genomes.” Genome Res. 15 (8). Cold Spring Harbor Laboratory:1034–50.
Zender, Charles S. 2016. “Bit Grooming: Statistically Accurate Precision-Preserving Quantization with Compression, Evaluated in the netCDF Operators (Nco, V4. 4.8+).” Geosci. Model Dev. 9 (9). Copernicus GmbH:3199–3211.