LangoScoley_Control_Sequence_Files

Dryad2016-01-01 更新2026-04-13 收录

基因变异分析

控制序列

数据链接：

http://datadryad.org/resource/doi:10.5061/dryad.k9b6f/3 数据链接链接失效反馈

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资源简介：

This folder contains the control sequences for the specific variants used for the analyses

创建时间：

2016-01-01

Additional file 3 of VariantscanR: an R-package as a clinical tool for variant filtering of known phenotype-associated variants in domestic animals

基因变异分析

表型关联

Additional file 3: Complete output of the variantscanR report for the 4 canine samples. Description of the data: Excel file containing the complete variantscanR output report, including 3 tables per s

DataCite Commons2024-08-14 更新110

gVCF_HG01277

基因组研究

基因变异分析

1000 Genomes gVCF mapped to hs37d5 for HG01277. Complete collection: https://doi.org/10.6084/m9.figshare.c.4414307

Figshare2019-04-09 更新50

MLH1 variants-defective DNA mismatch repair

遗传性疾病

基因变异分析

MLH1 heterodimerizes with PMS2 to form MutL alpha, a component of the post-replicative DNA mismatch repair system (MMR). This system assembles in a stepwise fashion, with the MutL complex recruited af

reactome.org50

gVCF_NA20867

基因组学

基因变异分析

1000 Genomes gVCF mapped to hs37d5 for NA20867. Complete collection: https://doi.org/10.6084/m9.figshare.c.4414307

DataCite Commons2020-08-27 更新100

Table2_Novel and recurrent genetic variants of VHL, SDHB, and RET genes in Chinese pheochromocytoma and paraganglioma patients.XLSX

肿瘤遗传学

基因变异分析

Background: Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors arising from chromaffin cells in the adrenal medulla and extra-adrenal ganglia, respectively. The study was aimed t

NIAID Data Ecosystem50

LangoScoley_Control_Sequence_Files

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