Murasaki is an anchor alignment program that is
exteremely fast (17 CPU hours for whole...rbitrarily parallelizable across multiple nodes using MPI)
memory efficient. (Even a single nod...
The accurate description and annotation of structural variants can be complex. This...own to the actual base pair positions. Furthermore, multiple rearrangements in a single are...
Development of cancer is driven by somatic alterations, including numerical and str...by array-Comparative Genomic Hybridization (CGH) or by (low-pass) whole genome sequencing (WGS). First, ‘GeneBreak’ col...
The MIRO (the miRNA omics) pipeline is a flexible and p...nerall short RNA) expression using short-read deep sequencing data. In its present implemen...the analysis of reads generated with the Illumina sequencing platform. MIRO allows to prep...
Metagenomics sequencing projects collect samples of DNA from uncharact...ical diversity present in a sample. The newest sequencing technologies have simultaneously made metagenomics easier, by making the sequencing process faster, and more diff...
...in the SK-BR-3 breast cancer cell line linking the genes CYTH1...nscriptome previously, genome sequencing did not identify a dire...n these two genes. After SMRT sequencing, Ribbon shows that there are...e gene fusions of this cancer cell line are investigated in Supplement...
Background: Transcriptomics, metabolomics, metagenomics, and other various next-generation sequencing (-omics) fields are kno...gh-dimensional numerical data as a colored grid of cells, efficiency and speed have often p...
The eFORGE tool provides a method to view the tissue specific regulatory component of...ed background DMPs. It assesses enrichment on a per cell type basis, since functional elements are differentially active in different cell types...
ART is a set of simulation tools to generate synthetic next-generation sequencing reads. ART simulates sequencing reads by mimicking real seque...rized from large recalibrated sequencing data. ART can also simulate r...or commercial next-generation sequencing platforms: Illumina's Solexa,...
...nces from high-throughput DNA sequencing reads.
Targeted bait capture...e starts with high-throughput sequencing reads (for example from Illum...ative paralogs, and calculate sequencing depth. For more information,&...n separately for each sample (single or paired-end sequence reads). Wh...