DecodeGenetics / BamHashLinks
☆37Updated 4 years ago
Alternatives and similar repositories for BamHash
Users that are interested in BamHash are comparing it to the libraries listed below
Sorting:
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- Wrapper for RTG's vcfeval; DEPRECATED!☆21Updated 9 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated 3 months ago
- ☆26Updated 4 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 5 months ago
- Population-scale detection of novel sequence insertions☆27Updated 2 years ago
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆24Updated 9 years ago
- Exploration of controlled loss of quality values for compressing CRAM files☆34Updated 2 years ago
- Integrated Variant Caller☆17Updated 7 years ago
- sort genomic data☆35Updated 5 years ago
- gvcf aggregation tool☆12Updated 7 years ago
- program for haplotype phasing from sequence reads and related tools☆25Updated 6 years ago
- picking up low allelic-fraction, somatic variants from tumor samples☆14Updated 7 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 5 months ago
- SV detection from paired end reads mapping☆38Updated 14 years ago
- FermiKit small variant calls for public SGDP samples☆17Updated 8 years ago
- An ultra fast and accurate paired-end adapter trimmer that needs no a priori adapter sequences.☆22Updated 4 years ago
- Structural variation and indel detection using rolling local string graph assembly☆9Updated 8 years ago
- Prioritize structural variants based on CADD scores☆29Updated 5 years ago
- Rapid competitive read demulitplexer. Made with tries.☆23Updated 2 weeks ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆56Updated 3 years ago
- Graphite - Graph-based variant adjudication☆28Updated 4 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆21Updated 3 years ago
- Scaffolding genomes using synthetic long read clouds☆20Updated 8 years ago
- simple library for dealing with SAM cigar strings☆41Updated 4 years ago
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Updated last year
- URMAP ultra-fast read mapper☆39Updated 4 years ago
- HPG Aligner is an ultrafast and highly sensitive Next-Generation Sequencing (NGS) mapper which supoprts both DNA and RNA alignment☆34Updated 7 years ago
- Browser based application for viewing bam alignments☆56Updated 8 years ago
- Hemang Parikh☆11Updated 9 years ago