Results for "DNA sequencing"
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...eted sequence capture, in which DNA sequencing libraries are enriched...sequences from high-throughput DNA sequencing reads. Targeted bait capture...ine starts with high-throughput sequencing reads (for example from Illum...utative paralogs, and calculate sequencing depth. For more information,&...2744 days ago
- Background. Next-generation sequencing technologies are now producing multiple times the genome size in tota...ence sequence. In this way, it can very quickly, and at no additional sequencing cost, generate new, modified...
2722 days ago
- EXCAVATOR2 is a collection of bash, R and Fortran scripts and codes that analyses Whole Exome Sequencing (WES) data to identify CNVs....ication of CNVs in small as well as large-scale re-sequencing population and cancer studies...
2718 days ago
- SWALO (scaffolding with assembly likelihood optimization) is a method for scaffolding based on likelihood of genome assemblies computed using generative models for sequencing. Download Git repository of SWALO is at https://github.com/atifrahman/SWALO.
2718 days ago
- SGA is a de novo genome assembler based on the concept of string graphs. The major goal of SGA is to be very memory efficient, which is achieved by using a compressed representation of DNA sequen...
2710 days ago
- Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads. Cutadapt helps with t...
2703 days ago
- The automated reconstruction of genome sequences in ancient genome analysis is a multifaceted process. EAGER en...rt tools for each step as well as new complementary tools tailored for ancient DNA data w...
2707 days ago
BIMA V3: an aligner customized for mate pair library sequencing
Summary: Mate pair library sequencing is an effective and economical method for detecting genomic structura...ccurate than popular NGS alignment programs when processing mate pair sequencing. Availability: http://bioinfo...2703 days ago
e-RGA: enhanced Reference Guided Assembly of Complex Genomes
Next Generation Sequencing has totally changed genomics: we are able to produce huge amounts of data at an incredibly low cost compared to Sanger sequencing. Despite this, some old probl...2699 days ago
GARM:Genome Assembly, Reconciliation and Merging
The pipeline is based mainly implemented using Perl scripts and modules and third-...ges contigs or scaffolds from different assemblers using the same or different sequencing technologies. When scaffolds...2699 days ago
