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Search results for structural variation variant calling

structural-variation x

variant-calling x

8 search results found

Fast and accurate gene fusion detection from RNA-Seq data

Paragraph ⭐ 140

Graph realignment tools for structural variants

Toolkit for calling structural variants using short or long reads

Bayestyper ⭐ 52

A method for variant graph genotyping based on exact alignment of k-mers

Population-wide Deletion Calling

Germline Dna ⭐ 23

A BioWDL variantcalling pipeline for germline DNA data. Starting with FASTQ files to produce VCF files. Category:Multi-Sample

Complex structural variant detection from WGS data

nRex: Germline and somatic single-nucleotide, short indel and structural variant calling

A scalable variant calling and benchmarking framework supporting both short and long reads.

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1-8 of 8 search results

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