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SRX21829903: wes
1 ILLUMINA (Illumina HiSeq 2500) run: 46.4M spots, 13.6G bases, 1.7Gb downloads

Design: Genomic DNA samples were collected and sequence libraries were constructed using the Agilent Sure Select Human Whole Exome V2 Kit (Agilent Technologies, Santa Clara, CA). Prepared libraries were sequenced using the HiSeq2500 System (Illumina, San Diego, CA). Reads obtained from the BWA software package (v. 0.7.15) was mapped with the human reference genome (GRCh37/hg19). Variant calling and variant annotation were performed using the Genome Analysis Toolkit (GATK)
Submitted by: Shengjing Hospital of China Medical University
Study: A novel CTBP1 mutation in a Chinese
Sample:
SAMN37475122 • SRS18929238 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: 22W001_case_C_W_Reorder_Sort_rmdup (1)
Instrument: Illumina HiSeq 2500
Strategy: Targeted-Capture
Source: GENOMIC
Selection: PCR
Layout: PAIRED
Runs: 1 run, 46.4M spots, 13.6G bases, 1.7Gb
Run# of Spots# of BasesSizePublished
SRR2611606846,443,30613.6G1.7Gb2023-09-20

ID:
29645735

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