首页/数据集/Homo sapiens Raw sequence reads

Homo sapiens Raw sequence reads

NIAID Data Ecosystem2026-04-25 收录

体细胞变异

测序深度性能评估

数据链接：

https://www.ncbi.nlm.nih.gov/sra/SRP222155 数据链接链接失效反馈

官方服务：

资源简介：

Systematic comparison of somatic variant calling performance among different sequencing depth and mutation frequency

应用场景：

创建时间：

2020-05-20

基因组学

体细胞变异

MAF files with the summary of the somatic variants identified on the exome of the cherry angioma and the healthy skin from outside the cherry angioma field.

DataCite Commons2025-06-30 更新100

Additional file 2 of Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series

体细胞变异

息肉研究

Additional file 2: Table S2. DNA variant profile (Case #2).

DataCite Commons2022-11-25 更新50

10 Synthetic Genomics Datasets

体细胞变异

基因组学基准测试

These are 10 synthetic genomics datasets generated with NEAT v3 (based on TP53 gene of Homo Sapiens) for the use case of benchmarking somatic variant callers. To find more about our generating framewo

NIAID Data Ecosystem40

Supplementary Material for: Higher Intercellular Variation in Genome-Wide Recombination Rate in Female Mice

基因组重组

体细胞变异

Meiotic recombination affects fertility, shuffles genomes, and modulates the effectiveness of natural selection. Despite conservation of the recombination pathway, the rate of recombination varies amo

DataCite Commons2021-09-10 更新70

Somatic variants identified in MSH3-deficient adenomas.

体细胞变异

DNA错配修复

This list contains all somatic variants identified in MSH3-deficient adenomas after the filtering process and before read check with Integrative Genome Viewer. (XLSX)

NIAID Data Ecosystem50

Homo sapiens Raw sequence reads

资源简介：

相关数据集