Whole genome sequencing (WGS) has transformed genomics by providing comprehensive insights into the genetic basis of human health and disease, surpassing targeted approaches. The decreasing cost of this technology has made it more accessible for clinical use, alongside advancements in sequencing and bioin...
Method data Ordering Resources Overview Recommended products—curated for whole genome sequencing Short workflow—create a normalized library pool in under 4 hours Low input, high complexity—up to 3-fold fewer duplicates from 1 ng of DNA when using the xGen DNA Library Prep Kit EZ Enzymatic ...
To assess the performance of PennCNV original algorithm for array data in whole genome sequencing data, we processed mapping (BAM) files to extract coverage, representing log R ratio (LRR) of signal intensity, and B allele frequency (BAF). We used high quality sample NA12878 from the ...
Our whole genome sequencing services use cutting-edge technologies and bioinformatics to deliver high-quality data and analysis for your genome of interest. Whether you are studying human, animal, plant, bacteria, or virus species, we have a range of WGS services to cater to your unique research...
The original sequencing data Experimental results Data analysis report Details in Whole Genome Sequencing for your writing (customization) For research purposes only, not intended for clinical diagnosis, treatment, or individual health assessments.
Whole-genome sequencing delivers a comprehensive view, ideal for discovery applications. Newer genome sequencers perform WGS more rapidly than ever.
M. et al. Inferring patient to patient transmission of Mycobacterium tuberculosis from whole genome sequencing data. BMC Infect. Dis. 13, 110 (2013). PubMed PubMed Central Google Scholar Shea, J. et al. Comprehensive whole-genome sequencing and reporting of drug resistance profiles on clinical...
In contrast to primary colorectal cancer (CRC) little is known about the genomic landscape of metastasized CRC. Here we present whole genome sequencing data of metastases of 429 CRC patients participating in the pan-cancer CPCT-02 study (NCT01855477). Un
Whole genome sequencing (WGS) offers an alternative data source to allow for the detection and characterization of the copy number across different genomic regions in a single experiment. A plethora of tools have been developed to utilize WGS data for CNV detection. None of these tools are ...
mityis a bioinformatic analysis pipeline designed to call mitochondrial SNV and INDEL variants from Whole Genome Sequencing (WGS) data.mitycan: identify very low-heteroplasmy variants, even <1% heteroplasmy when there is sufficient read-depth (eg >1000x) ...