相关实验视频

Updated: Jun 7, 2026

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
14:06

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

Published on: June 23, 2012

15.3K

AdmixPipe v3:从SNP数据中促进人口结构划分

Steven M Mussmann1,2, Marlis R Douglas1, Tyler K Chafin1,3

  • 1Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701, United States.

Bioinformatics advances
|December 4, 2023
PubMed
概括

AdmixPipe v3通过将流行的软件集成到单一管道中来简化人口遗传分析. 这种生物信息学工具提高了研究遗传集群的研究人员的可复制性和可访问性.

更多相关视频

Infinium Assay for Large-scale SNP Genotyping Applications13:33

Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

39.0K
Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

10.2K

相关概念视频

Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...