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Additional file 4 of Low-cost and clinically applicable copy number profiling using repeat DNA

NIAID Data Ecosystem2026-03-13 收录

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https://figshare.com/articles/dataset/Additional_file_4_of_Low-cost_and_clinically_applicable_copy_number_profiling_using_repeat_DNA/20508393 数据链接链接失效反馈

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Additional file 4 Supplementary Table S4

应用场景：

创建时间：

2022-08-17

基因组学

拷贝数变异

Table S7. Information about QTLs found to be overlapped with CNVRs identified in the present study. (XLSX 104 kb)

Mendeley Data2024-06-25 更新160

Additional file 6 of Identification and population genetic analyses of copy number variations in six domestic goat breeds and Bezoar ibexes using next-generation sequencing

群体遗传学

拷贝数变异

Additional file 6: Table S4. Significantly enriched terms for the genes overlapped with 2394 CNVRs identified in seven goat populations.

DataCite Commons2024-02-13 更新90

Exome sequencing data analysis to characterize rare germline copy number variants involved in colorectal cancer predisposition

结直肠癌遗传易感性

拷贝数变异

Colorectal cancer (CRC) represents the third most common cancer worldwide. Next generation sequencing (NGS) appearance has allowed us to produce huge amount of data and, in order to fully exploit its

NIAID Data Ecosystem80

Mouse SCLC tumors were analysed by whole exome sequencing and used to obtain DNA copy number profiles using ENCODER.. ENCODER-validation mouse sample

癌症基因组数据

拷贝数变异

Current methods for the detection of copy number aberrations (CNA) from whole-exome sequencing (WES) data use the depth of coverage of captured exons only. Accurate CNA determination is complicated by

NIAID Data Ecosystem110

Number of CNVs per person detected in 96 subjects by each algorithm.

拷贝数变异

精神分裂症遗传研究

See Table 2 for explanation of algorithms. a4 control and 5 schizophrenia subjects with no identified CNVs. b6 control and 6 schizophrenia subjects with no identified CNVs. c1 control and 2 schizophre

NIAID Data Ecosystem80

Additional file 4 of Low-cost and clinically applicable copy number profiling using repeat DNA

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