Topic: cram Goto Github
Some thing interesting about cram
Some thing interesting about cram
cram,Using ChatGPT & GPT-4 to generate CRAM & PyCRAM designators in a one-shot fashion
Organization: ag-sc
cram,Rust software for solving impartial games.
User: beling
cram,Fast and accurate sequence demultiplexing
Organization: biosails
cram,basepair bio: a single binary with many useful genomics subtools.
User: brentp
cram,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).
Organization: computational-genomics-bsc
cram,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.
Organization: computational-genomics-bsc
cram,cram is a computational room acoustics module to simulate and explore various acoustic properties of a modeled space
User: gregzanch
Home Page: https://cram.vercel.app/
cram,VerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.
User: griffan
Home Page: http://griffan.github.io/VerifyBamID/
cram,Machinekit configuration for the Fabrikator Mini + CRAMPS board
User: machinekoder
cram,A script to report depth of coverage from BAM/SAM/CRAM file or parse the output generated from "samtools depth"
User: maurya-anand
cram,ILIAD: A suite of automated Snakemake workflows for processing genomic data for downstream applications
User: ncherric
Home Page: https://iliad.readthedocs.io/
cram,A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
Organization: nf-cmgg
Home Page: https://nf-cmgg.github.io/germline/
cram,A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
Organization: nf-cmgg
Home Page: https://nf-cmgg.github.io/structural/
cram,Convert output from Cram (and some other tools) to TAP (Test Anything Protocol)
User: nikolausschueler
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