R tools to mine & craft somatic mutations from cancer genomes
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Updated
May 23, 2017 - R
R tools to mine & craft somatic mutations from cancer genomes
Updated Reference Genome Sequence and Annotation of Mycobacterium bovis AF2122/97
probability emitting pangenome graphs
🔪⛓️ Repair nanopore assemblies using related genome(s)
Explore eukaryotic genome composition and organization with iLoci
Calling SNPs using TASSEL GBS V2 pipeline for ponderosa pine using the reference genome of loblolly pine
Get Started with DNA Sequencing working with .FastQ and .FastA file formats and performing Pattern Matching Algorithms (Exact & Approximate).
Repository including scripts and workflows for "Investigating the impact of reference assembly choice on genomic analyses in a cattle breed"
An ultrafast and highly sensitive Next-Generation Sequencing (NGS) read mapper and methylation extractor.
Serves a web interface and RESTful API for reference genome assets.
A Python object for standardized reference genome assets.
Analysis documentation for part of the reference genome assembly of the humble guinea pig. Oxford Nanopore Technologies (ONT) pore-c data.
Numerical Encoding for Human Genetic Variants
Create required reference genome index files for WGS data analysis
Telomere-2-Telomere Genome from Saudi Arabia
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