Results for "B"
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...nucleotide-resolution analysis of structural variants More at http://bioinform.github.io/breakseq2/ Download Break...q2/archive/2.2.tar.gzFor other versions, see "releases". https://github.com/bioinform/breakseq2/relea...3048 days ago
Pattern Searching in a Single Genome
Pattern searching holds much importance for biologists , for the understanding of DNA ( and its functionality) can be more than a matter of satisfying curiosity , but also give answers to many i...3042 days ago
- ...anipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF. These file fo...n on this page is targeted at end-users. For developers, the source code, building instructions and imple...
2989 days ago
- GA4GH Data Working Group Led by David Haussler (UCSC) and Richard Durbin (Sanger Institute), the Data Working Group (DWG) of the Global Alliance brings together th...ers with IT industry leaders to create global standards and tools for the...
3028 days ago
RNA-Seq De novo Assembly Using Trinity
Trinity, developed at the Broad Institute and the Hebrew University of Jerusalem, r...les: Inchworm, Chrysalis, and Butterfly, applied sequentially...erived from paralogous genes. Briefly, the process works like...g these disjoint graphs. Butterfly then processes the in...3026 days ago
- Easyfig has moved to github, for newer releases of Easyfig please visit our new webpage - https://mjsull.github.io/Easyfig. Easyfig is a Python application for creating linear comparison figures of multiple genomic...
2989 days ago
Awesome bioinformatics pipelines !
A curated list of awesome pipeline toolkits ... https://github.com/pditommaso/awesome-pipeline3018 days ago
PhyloGrapher - Graph Visualization Tool
PhyloGrapher is a program designed to visualize and study evol...mologous genes or proteins (elements).PhyloGrapher is a drawing tool that gene...for a given set of elements. In general, it is possible to use PhyloGrapher&nb...3011 days ago
PAired-eND Assembler for DNA sequences
PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the sequence, and reconstruct an overlapping sequence. More at https://github.com/neufeld/pandaseq3012 days ago
- ...ST/RNASeq projects. MIRA assembles/maps reads gained by...(in development) Pacific Biosciences sequencing i...ogies either in a single assembly run (a true hybrid assembly...the past 14 years to get assembly jobs I work on done efficie...
3012 days ago
