All data used in this study are available for further open-science investigation. Whole-genome sequencing (WGS) is gradually replacing whole-exome sequencing and chromosomal microarray analysis (CMA) ...

This test marks Tempus’ first foray into adopting whole-genome sequencing (WGS) as a platform, supporting clinicians with detection of all clinically-relevant variants and advancing the landscape of ...

Here, we explored the possibility that non-target reads from plant DNA sequencing can serve as phenotyping proxies for addressing such questions. We used data from a whole-genome and -epigenome ...

Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing ...

Methods: We have implemented a genetic test to identify the presence of this variant in the biological samples that are presently collected for anti-doping analysis (whole blood ... and the aims of ...

Once done, it is put together using the tags to create a whole genome — in the same ... an Indian dataset helps identify new variants. The researchers have identified 135 million genetic variations in ...

my ($id1, $flag1, $chr_from1, $loc_from1, $mapq1, $cigar1, $d1_1, $d2_1, $d3_1, $read1, $read_qual1, @rest1) = split(/\t/, $line1); my ($id2, $flag2, $chr_from2, $loc ...

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