statgen / verifyBamIDLinks
☆28Updated 8 years ago
Alternatives and similar repositories for verifyBamID
Users that are interested in verifyBamID are comparing it to the libraries listed below
Sorting:
- create a gemini-compatible database from a VCF☆55Updated 5 years ago
- Tools for bam file processing☆55Updated 10 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated 2 months ago
- BigWig manpulation tools using libBigWig and htslib☆30Updated last year
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆25Updated 9 years ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆40Updated 2 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated last month
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆58Updated 3 years ago
- (WIP) best-practices workflow for rare disease☆62Updated last year
- simple library for dealing with SAM cigar strings☆41Updated 4 years ago
- Prioritize structural variants based on CADD scores☆29Updated 5 years ago
- Genomic VCF to tab-separated values☆48Updated 2 years ago
- FermiKit small variant calls for public SGDP samples☆17Updated 9 years ago
- Integrated Variant Caller☆17Updated 7 years ago
- ☆36Updated 5 years ago
- Numerical Encoding for Human Genetic Variants☆42Updated 2 years ago
- Samwell: a python package for using genomic files... well☆20Updated 3 years ago
- Benchmark pipeline for Structural Variation analyses, funded by the ALLBio.☆24Updated 11 years ago
- A method to identify structural variation from sequencing data in target regions☆32Updated 5 years ago
- a pileup library that embraces the huge☆43Updated 5 years ago
- ☆24Updated 8 months ago
- ☆23Updated 2 weeks ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- A utility for merging and genotyping Illumina-style GVCFs.☆33Updated 6 years ago
- adds sample names and read-group (RG) tags to BAM alignments☆51Updated 5 years ago
- Bam Read Index - Extract alignments from a bam file by readname☆28Updated last year
- v2.x of the microassembly based somatic variant caller☆23Updated 6 months ago
- What's The Function of these genes?☆22Updated 8 years ago
- Mapping-free variant caller for short-read Illumina data☆20Updated 5 years ago
- Structural Variant Prediction Viewer☆35Updated 8 years ago