2592 days ago
NovelSeq: Novel Sequence Insertion Detection
The NovelSeq framework is designed to detect novel sequence insertions using high throughput paired-end whole genome sequencing data. http://novelseq.sourceforge.net/Home Paper at https://www.ncbi.nlm.nih.gov/pubmed/203857262586 days ago
GraphMap - A highly sensitive and accurate mapper for long, error-prone reads
...sp; Mapping position agnostic to alignment parameters. Co...es and sequencing technologies even with default parameters. Ci...create de novo assemblies from raw nanopore and PacBio reads without requiring e...2588 days ago
Genetic-mapper: SVG Genetic Map Drawer
...t least the marker name (ID), linkage group (LG) and the position (POS) separeted by tabulations. Additionally a logarithm of odds (LOD score) can be provided. Any extra parameter will be ignored. map....2577 days ago
2576 days ago
2551 days ago
DarkHorse: a method for genome-wide prediction of horizontal gene transfer
A new approach to rapid, genome-wide identification and ranking of horizontal transfer candidate proteins is presented. The method is quantitative, reproducible, and...2573 days ago
eQuant : energy-based quality assessment of protein
...quality. Especially, in-silico modeled structures are prone to contain serious errors, which limit the usefulness and reliability of these particular protein structures.eQ...2571 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...ent cross-cohort RNA- and small-RNA-Seq studies span tens of replicates and batch...A-Seq. UMI support in Strand NGS is end-to-end, spanning alignment to variant cal...a premier life science informatics innovation company. Founded in 2000, Strand is...2450 days ago
2570 days ago