zicofish / secramLinks
A library for compressing, encrypting, and querying alignment data.
☆15Updated 9 years ago
Alternatives and similar repositories for secram
Users that are interested in secram are comparing it to the libraries listed below
Sorting:
- Predict the functional consequences of both coding and non-coding single nucleotide variants (SNVs)☆20Updated 4 years ago
- ☆10Updated 8 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- vcf file manipulation☆22Updated 10 years ago
- Allele frequency filtering for Mendelian variant discovery☆18Updated 9 years ago
- Allele frequency filter app☆14Updated 3 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- ☆36Updated 5 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 10 months ago
- GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS☆17Updated 6 years ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Updated 7 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Updated 7 years ago
- NExt generation Analysis Toolbox☆14Updated 10 years ago
- Genomic VCF to tab-separated values☆47Updated 2 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 5 years ago
- R package for extracting mutation signatures from a list of somatic mutations☆37Updated 6 years ago
- A collection of well-known bioinformatics programs.☆25Updated 10 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- A talk on Makesfiles in bioinformatics☆26Updated 12 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- High-definition reconstruction of clonal composition from next-generation sequencing data☆41Updated 9 years ago
- Docker image of JBrowse Genome Browser☆15Updated 4 years ago
- a wee tool for random access into BGZF files.☆85Updated 7 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 10 months ago
- Tools for producing pseudo-cgh of next-generation sequencing data☆18Updated 9 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- ☆26Updated 5 years ago
- A library for manipulating bioinformatics sequencing formats in Apache Spark☆32Updated 2 months ago
- conda recipes for genomic data☆84Updated 4 years ago
- Call regions of homozygosity and make tentative UPD calls☆12Updated 4 months ago