Command-line program to wrap dagchainer and combine pairwise results into multi-alignments in column format
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Updated
Oct 15, 2010 - C++
Command-line program to wrap dagchainer and combine pairwise results into multi-alignments in column format
Consensus calling (or "reference assisted assembly"), chiefly of ancient mitochondria
A WGS de novo assembler based on the FMD-index for large genomes
Generate visualizations of whole genomes or small sequences
firefox addon : IGV (Integrative Genomics Viewer) control through mozilla Firefox
Predicting Tissue Specific Enhancer Activity from Epigenetic Marks and Sequence
From second generation sequencing reads to annotated bacterial genome
From second generation sequencing reads to variant calls
Simple Java code for sequence alignment and scoring, built on top of biojava-alignment.
Several computational genomics projects
GenomeDiff (*.gd) file parser for Node.js
Simple wrapper for the GWAS Catalog
A Python package for Biopython that gives feature annotations from GenBank records a new and better life
Genome scaffolding and phasing with Hi-C using a genetic algorithm approach.
A prototype framework for expressing automated laboratory protocols originally targeting the Transcriptic API
High-performance error correction for Illumina resequencing data
Rank Aggregation in Phenotypic Selection
Tools for producing pseudo-cgh of next-generation sequencing data
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