Can I analyze VCF data for my whole exome/whole genome sequence analysis project? Yes, you can analyze both raw sequencing data as well as VCF variant data for genome resequencing projects in Lasergene. When starting from VCF data, Lasergene will classify called variants by their effect on ...
Here, we examine the full allelic spectrum with plasma lipids using whole genome sequences and harmonized lipids from the National Heart, Lung, and Blood Institute (NHLBI) Trans-Omics for Precision Medicine (TOPMed) program17,18. We studied 66,329 participants and 428 million variants across mult...
PacBio whole genome sequencing analysis solutions allow you to generate gold-standard reference genomes through de novo assembly, phase haplotypes and call all structural variant types.
et al. Whole genome sequence analysis of a large isoniazid-resistant tuberculosis outbreak in London: a retrospective observational study. PLOS Med. 13, e1002137 (2016). PubMed PubMed Central Google Scholar Feuerriegel, S. et al. PhyResSE: a web tool delineating Mycobacterium tuberculosis ...
Whole genome sequencing (WGS) is the comprehensive read and analysis of an entire genome, including non-coding regions of the genome.
Whole-genome sequencing delivers a comprehensive view, ideal for discovery applications. Newer genome sequencers perform WGS more rapidly than ever.
Objectives: The objectives of this study were to identify antimicrobial resistance genotypes for Campylobacter and to evaluate the correlation between resistance phenotypes and genotypes using in vitro antimicrobial susceptibility testing and whole-genome sequencing (WGS). Methods: One hundred-fourteen Campylob...
Availability of whole genome sequence and its functional analysis will aid in the process of genetic manipulation to develop FC II as a cell factory for production of biofuel and industrially important molecules. Acknowledgement We thank of Gagva operation team of RIL for all growth and cultivation...
Genome sequence analysis of the 10 clinical strains revealed that the draft genome sequences of eight clinical M. pneumoniae strains isolated in 2012 were similar in size (800, 977 to 807, 092 bp); however, the strains isolated in 2010 had smaller genomes (777, 576 bp for CIP10349 and ...
Generate complete genome assemblies using long nanopore sequencing reads. Resolve structural variants, repeats, phasing, and base modifications.