cram
There are 23 repositories under cram topic.
samtools/htslib
C library for high-throughput sequencing data formats
samtools/htsjdk
A Java API for high-throughput sequencing data (HTS) formats.
divonlan/genozip
A modern compressor for genomic files (FASTQ, SAM/BAM/CRAM, VCF, FASTA, GFF/GTF/GVF, 23andMe...), up to 5x better than gzip and faster too
Griffan/VerifyBamID
VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.
chrovis/cljam
A DNA Sequence Alignment/Map (SAM) library for Clojure
sbslee/fuc
Frequently used commands in bioinformatics
gregzanch/cram
cram is a computational room acoustics module to simulate and explore various acoustic properties of a modeled space
ncherric/Iliad
ILIAD: A suite of automated Snakemake workflows for processing genomic data for downstream applications
biosails/pheniqs
Fast and accurate sequence demultiplexing
prysk/prysk
Functional tests for command line applications
nf-cmgg/structural
A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
nf-cmgg/germline
A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
brentp/bpbio
basepair bio: a single binary with many useful genomics subtools.
brentp/bedder-rs
an API for intersections of genomic data
ag-sc/CRAM-Generation-LLM
Using ChatGPT & GPT-4 to generate CRAM & PyCRAM designators in a one-shot fashion
beling/impartial-games
Rust software for solving impartial games.
Computational-Genomics-BSC/GenomeMosaicMaker
Tool for copying read-alignments regions centered around variants (in VCF/VCF.GZ/BCF format) from existing genomes (in SAM/BAM/CRAM format) to insert them into canvas genomes (in SAM/BAM/CRAM format).
Computational-Genomics-BSC/GenomeVariator
Tool for adding genomic variants to an existing genome (in SAM/BAM/CRAM format). Currently supported variants are SNVs, indels and SVs (insertions, deletions, translocations, inversions and duplications). It generates realistic genomes as almost always less than 99% of the original real genome is modified.
machinekoder/Fabrikator-Mini-CRAMPS
Machinekit configuration for the Fabrikator Mini + CRAMPS board
maurya-anand/getBamDepth
A script to report depth of coverage from BAM/SAM/CRAM file or parse the output generated from "samtools depth"
REGOVAR/Pirus
a REST service to launch pipeline
mtso/cram
Line cramming/un-cramming utility
nikolausschueler/tapconverters
Convert output from Cram (and some other tools) to TAP (Test Anything Protocol)