SNV calling from NGS data is any of a range of methods for identifying the existence of single nucleotide variants (SNVs) from the results of next generation...
23 KB (3,217 words) - 01:27, 3 December 2023
Single-nucleotide polymorphism (category Short description is different from Wikidata)
Single-base extension SNP array SNP genotyping SNPedia Snpstr SNV calling from NGS data Suspension array technology Tag SNP TaqMan Variome "single-nucleotide...
58 KB (6,250 words) - 19:03, 19 December 2024
Cancer genome sequencing (section Data Analysis)
medicine Pyrosequencing Single molecule real time sequencing SNV calling from NGS data Samuel Levy; et al. (October 2007). "The Diploid Genome Sequence...
29 KB (3,085 words) - 22:03, 2 December 2023
John G. Cleary (category Short description is different from Wikidata)
recognition, sequence alignment, SNV calling from NGS data, and various problems in metagenomics. Cleary worked from 1999 to 2001 with Webmind, Inc. Cleary...
7 KB (576 words) - 05:19, 18 July 2023
Single-cell sequencing (category Short description is different from Wikidata)
or frozen tumors may be analyzed and categorized with respect to SCNAs, SNVs, and rearrangements quite well using whole-genome DNAS approaches. Cancer...
74 KB (8,560 words) - 21:49, 12 December 2024
Human genome (category Articles using infobox templates with no data rows)
genetic disorder. Copy number variants (CNVs) and single nucleotide variants (SNVs) are also able to be detected at the same time as genome sequencing with...
99 KB (10,142 words) - 15:38, 13 October 2024