• Stars
    star
    105
  • Rank 317,856 (Top 7 %)
  • Language
    Rust
  • License
    MIT License
  • Created over 2 years ago
  • Updated about 1 year ago

Reviews

There are no reviews yet. Be the first to send feedback to the community and the maintainers!

Repository Details

using all the bits for echt rapid variant annotation and filtering

Echtvar: Really, truly rapid variant annotation and filtering

Rust

Echtvar efficiently encodes variant allele frequency and other information from huge population datasets to enable rapid (1M variants/second) annotation of genetic variants. It chunks the genome into 1<<20 (~1 million) bases, encodes each variant into a 32 bit integer (with a supplemental table for those that can't fit due to large REF and/or ALT alleles). It uses the zip format, delta encoding and integer compression to create a compact and searchable format of any integer, float, or low-cardinality string columns selected from the population file.

read more at the why of echtvar

Getting started.

Get a static binary and pre-encoded echtvar files for gnomad v3.1.2 (hg38) here: https://github.com/brentp/echtvar/releases/latest That page contains exact instructions to get started with the static binary.

⬇️Download or Build instructions for linux

The linux binary is available via:

wget -O ~/bin/echtvar https://github.com/brentp/echtvar/releases/latest/download/echtvar \
    && chmod +x ~/bin/echtvar \
    && ~/bin/echtvar # show help

Users can make their own echtvar archives with echtvar encode, and pre-made archives for gnomAD version 3.1.2 are here

Rust users can build on linux with:

cargo build --release --target x86_64-unknown-linux-gnu

To run echtvar with an existing archive (we have several available in releases) is as simple as

echtvar anno -e gnomad.echtvar.zip -e other.echtvar.zip input.vcf output.annotated.bcf

an optional filter that utilizes fields available any of the zip files can be added like:

-i "gnomad_popmax_af < 0.01"

echtvar can also accept input from stdin using "-" or "/dev/stdin" for the input argument.

usage

encode

make (encode) a new echtvar file. This is usually done once (or download from those provided in the Release pages) and then the file can be re-used for the annotation (echtvar anno) step with each new query file. Note that input VCFs must be decomposed.

echtvar \
   encode \
   gnomad.v3.1.2.echtvar.zip \
   conf.json # this defines the columns to pull from $input_vcf, and how to
   $input_population_vcf[s] \ can be split by chromosome or all in a single file.
name and encode them

See below for a description of the json file that defines which columns are pulled from the population VCF.

annotate

Annotate a decomposed (and normalized) VCF with an echtvar file and only output variants where gnomad_af from the echtvar file is < 0.01. Note that multiple echtvar files can be specified and the -i expression is optional and can be elided to output all variants.

echtvar anno \
   -e gnomad.v3.1.2.echtvar.v2.zip \
   -e dbsnp.echtvar.zip \
   -i 'gnomad_popmax_af < 0.01' \
   $cohort.input.bcf \
   $cohort.echtvar-annotated.filtered.bcf

Configuration File for Encode

When running echtvar encode, a json5 (json with comments and other nice features) determines which columns are pulled from the input VCF and how they are stored.

A simple example is to pull a single integer field and give it a new name (alias):

[{"field": "AC", "alias": "gnomad_AC"}]

This will extract the "AC" field from the INFO and labeled as "gnomad_AC" when later used to annotate a VCF. Note that it's important to give a description/unique prefix lke "gnomad_" so as not to collide with fields already in the query VCF.

⬇️Expand this section for detail on additional fields, including float and string types
[
    {"field": "AC", "alias": "gnomad_AC"},
    // this JSON file is json 5 and so can have comments
    // the missing value will default to -1, but the value: -2147483648 will
    // result in '.' as it is the missing value for VCF.
    {"field": "AN", "alias":, gnomad_AN", missing_value: -2147483648},
    {
           field: "AF",
           alias: "gnomad_AF",
           missing_value: -1,
           // since all values (including floats) are stored as integers, echtvar internally converts
           // any float to an integer by multiplying by `multiplier`.
           // higher values give better precision and worse compression.
           // upon annotation, the score is divided by multiplier to give a number close to the original float.
           multiplier: 2000000,
           // set zigzag to true if your data has negative values
           zigzag: true,
   }
    // echtvar will save strings as integers along with a lookup. this can work for fields with a low cardinality.
    {"field": "string_field", "alias":, gnomad_string_field", missing_string: "UNKNOWN"},
    // "FILTER" is a special case that indicates that echtvar should extract the FILTER column from the annotation vcf.
    {"field": "FILTER", "alias": "gnomad_filter"},
]

The above file will extract 5 fields, but the user can chooose as many as they like when encoding. All fields in an echtvar file will be added (with the given alias) to any VCF it is used to annotate.

Other examples are available here

And full examples are in the wiki

Expressions

An optional expression will determine which variants are written. It can utilize any (and only) integer or float fields present in the echtvar file (not those present in the query VCF). An example could be:

-i 'gnomad_af < 0.01 && gnomad_nhomalts < 10'

The expressions are enabled by fasteval with supported syntax detailed here.

In brief, the normal operators: (&&, ||, +, -, *, /, <, <=, >, >= and groupings (, ), etc) are supported and can be used to craft an expression that returns true or false as above.

References and Acknowledgements

Without these (and other) critical libraries, echtvar would not exist.

echtvar is developed in the Jeroen De Ridder lab

More Repositories

1

cyvcf2

cython + htslib == fast VCF and BCF processing
Cython
356
star
2

vcfanno

annotate a VCF with other VCFs/BEDs/tabixed files
Go
332
star
3

goleft

goleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
Go
202
star
4

slivar

genetic variant expressions, annotation, and filtering for great good.
Nim
189
star
5

smoove

structural variant calling and genotyping with existing tools, but, smoothly.
Go
187
star
6

bio-playground

miscellaneous scripts for bioinformatics/genomics that dont merit their own repo.
C
181
star
7

somalier

fast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
Nim
180
star
8

hts-nim

nim wrapper for htslib for parsing genomics data files
Nim
149
star
9

cruzdb

python access to UCSC genomes database
Python
129
star
10

peddy

genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF
Jupyter Notebook
122
star
11

bwa-meth

fast and accurate alignment of BS-Seq reads using bwa-mem and a 3-letter genome
Python
116
star
12

jigv

igv.js standalone page generator and automatic configuration to view bam/cram/vcf/bed. "working in under 1 minute"
Nim
107
star
13

combat.py

python / numpy / pandas / patsy version of ComBat for removing batch effects.
Python
98
star
14

intintmap

fast int64-int64 map for go
Go
93
star
15

duphold

don't get DUP'ed or DEL'ed by your putative SVs.
Nim
90
star
16

slurmpy

submit jobs to slurm with quick-and-dirty python
Python
88
star
17

pyfasta

fast, memory-efficient, pythonic (and command-line) access to fasta sequence files
Python
86
star
18

vcfgo

a golang library to read, write and manipulate files in the variant call format.
Go
65
star
19

fishers_exact_test

Fishers Exact Test for Python (Cython)
Python
60
star
20

xopen

open files for buffered reading and writing in #golang
Go
60
star
21

interlap

fast, pure-python interval overlap testing
Python
50
star
22

seqcover

seqcover allows users to view coverage for hundreds of genes and dozens of samples
Nim
49
star
23

rare-disease-wf

(WIP) best-practices workflow for rare disease
Nextflow
49
star
24

hts-python

pythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)
Python
49
star
25

go-chartjs

golang library to make https://chartjs.org/ plots (this is vanilla #golang, not gopherjs)
Go
47
star
26

hts-nim-tools

useful command-line tools written to showcase hts-nim
Nim
46
star
27

irelate

Streaming relation (overlap, distance, KNN) of (any number of) sorted genomic interval sets. #golang
Go
45
star
28

bsub

python wrapper to submit jobs to bsub (and later qsub)
Python
43
star
29

combined-pvalues

combining p-values using modified stouffer-liptak for spatially correlated results (probes)
Python
40
star
30

align

sequence alignment. global, local, glocal.
Python
40
star
31

bigly

a pileup library that embraces the huge
Go
39
star
32

indelope

find large indels (in the blind spot between GATK/freebayes and SV callers)
Nim
39
star
33

tiwih

simple bioinformatics command-line (t)ools (i) (w)ished (i) (h)ad.
Nim
39
star
34

cigar

simple library for dealing with SAM cigar strings
Python
37
star
35

gsort

sort genomic data
Go
35
star
36

450k-analysis-guide

A Practical (And Opinionated) Guide To Analyzing 450K Data
TeX
34
star
37

geneimpacts

prioritize effects of variant annotations from VEP, SnpEff, et al.
Python
31
star
38

quicksect

a cythonized, extended version of the interval search tree in bx
Python
30
star
39

poverlap

significance testing over interval overlaps
Python
29
star
40

fastbit-python

pythonic access to fastbit
Python
26
star
41

nim-lapper

fast easy interval overlapping for nim-lang
Nim
24
star
42

lua-stringy

fast lua string operations
C
21
star
43

pybloomfaster

fast bloomfilter
C
21
star
44

vcfassoc

perform genotype-phenotype-association tests on a VCF with logistic regression.
Python
20
star
45

toolshed

python stuff I use
Python
19
star
46

bw-python

python wrapper to dpryan79's bigwig library using cffi
C
19
star
47

methylcode

Alignment and Tabulation of BiSulfite Treated Reads
C
16
star
48

tnsv

add true-negative SVs from a population callset to a truth-set.
Nim
15
star
49

hileup

horizontal pileup
C
15
star
50

nim-kmer

DNA kmer operations for nim
Nim
15
star
51

genoiser

use the noise
Nim
15
star
52

bigwig-nim

command-line querying+conversion of bigwigs and a nim wrapper for dpryan's libbigwig
Nim
15
star
53

vcf-bench

evaluating vcf parsing libraries
Zig
14
star
54

agoodle

numpy + GDAL == agoodle
Python
13
star
55

hts-zig

ziglang + htslib
Zig
12
star
56

aclust

streaming, flexible agglomerative clustering
Python
12
star
57

gobio

miscellaneous script-like stuff in go for bioinformatics
Go
12
star
58

excord

extract SV signal from a BAM
Go
11
star
59

fastahack-python

cython wrapper to fastahack
C++
11
star
60

gobe

a fast, interactive, light-weight, customizable, web-based comparative genomics viewer with simple text input format.
Haxe
10
star
61

spacepile

convert reads from repeated measures of same piece of DNA into spaced matricies for deep learners.
Rust
10
star
62

bwa-mips

Map sequence from Molecular Inversion Probes with BWA, strip arms, de-dup, ..., profit
Python
10
star
63

bix

tabix file access with golang using biogo machinery
Go
9
star
64

sveval

run multiple sv evalution tools
Python
8
star
65

clinical-components

Summarize the clinical (or lab) components and correlations of your dataset.
Python
8
star
66

bowfast

run bowtie then bfast on colorspace reads.
Shell
7
star
67

bcf

bcf parsing in golang
Go
7
star
68

inheritance

inheritance models for mendelian diseases
Python
7
star
69

bamject

DO NOT USE inject variants (snps/indels) from a vcf into a bam efficiently.
Nim
7
star
70

skidmarks

find runs (non-randomness) in sequences
Python
7
star
71

falas

Fragment-Aware Local Assembly for Short-reads
Nim
7
star
72

bpbio

basepair bio: a single binary with many useful genomics subtools.
Nim
6
star
73

kexpr-nim

nim wrapper for Heng Li's kexpr math expression evaluator library
C
5
star
74

go-blosc

go wrapper for blosc (blocked number compression with fast random access)
Go
5
star
75

clustermodel

fitting models to clustered correlated data
Python
5
star
76

celltypes450

adjust for cell-type composition in 450K data using houseman's and other methods.
R
5
star
77

crystal

find clusters and model correlated data from DNA methylation and other genomic sources.
Python
5
star
78

variantkey-nim

nim-wrapper for variantkey -- (chrom, pos, ref, alt) -> uint64
C
4
star
79

pedfile

pedigree file parsing and relatedness calculations for nim
Nim
4
star
80

shuffler

shuffle genome regions to determine probability of user-defined metric
Python
4
star
81

go-giggle

golang wrapper to giggle
Go
4
star
82

bedder-rs

an API for intersections of genomic data
Rust
4
star
83

nim-gzfile

simple reader and writer for gzipped (and regular) files
Nim
4
star
84

find_cns

find conserved non-coding sequences (CNS)
Python
4
star
85

nim-cgranges

nim wrapper for https://github.com/lh3/cgranges for faster interval tree
C
3
star
86

d4-nim

nim-lang wrapper for https://github.com/38/d4-format
Nim
3
star
87

faidx

faidx for golang
Go
3
star
88

flatfeature

python module for dealing with BED format for genomic data as a numpy array.
Python
3
star
89

tabix-py

interface to tabix using cffi
C
3
star
90

4bit

4bit fasta format.
C
3
star
91

ksw2-nim

nim wrapper for lhs/ksw2 for fast smith-waterman
C
3
star
92

htsuse

some C stuff that uses htslib
C
2
star
93

nim-minizip

nothing to see here.
C
2
star
94

pyfastx

unified access to fasta, fastx using kseq.h + ??
C
2
star
95

learnflash

all the stuff i want to remember how to do in haxe / flash
2
star
96

ififo

ififo provides a fast, sized, generic thread-safe FIFO in golang.
Go
2
star
97

dotfiles

my .bash, .vim, .* files
Shell
2
star
98

cysolar

copy of pysolar using cython
Python
2
star
99

cgotbx

yeah, another tabix wrapper for go.
Go
1
star
100

totable

simple python / cython wrapper to tokyo cabinet tables
C
1
star