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SRX22108328: WXS of Peripheral Blood:Czech Dysplasia
1 ILLUMINA (Illumina NovaSeq 6000) run: 49.6M spots, 14.9G bases, 4.3Gb downloads

Design: The qualified DNA samples were first randomly broken into fragments of 150 bp -220 bp by Covaris, and the library was constructed and captured using the Agilent SureSelect Human All Exon V7 reagent kit. The DNA fragments underwent terminal repair, ployA tail addition, sequencing connector addition, purification, magnetic bead capture, PCR amplification, and other steps to finally complete the library construction
Submitted by: Guanghua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Study: Whole Exome Sequencing of Czech Dysplasia in a Chinese pedigree
show Abstracthide Abstract
Czech dysplasia is a rare skeletal dysplasia with symptomology including platyspondyly, brachydactyly of the third and fourth toes, and early-onset of progressive pseudorheumatoid arthritis. The disorder segregates in an autosomal dominant fashion. A specific missense mutation (c.823C > T, R275C) in exon 13 of the COL2A1 gene has been identified in German and Japanese families. Whole-exome sequencing (WES) identified the COL2A1 missense mutation (c.823 C>T, R275C) in a Chinese familiy.
Sample: case
SAMN37851305 • SRS19173211 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: 19R24738
Instrument: Illumina NovaSeq 6000
Strategy: WXS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Runs: 1 run, 49.6M spots, 14.9G bases, 4.3Gb
Run# of Spots# of BasesSizePublished
SRR2640259849,640,89614.9G4.3Gb2023-10-16

ID:
30040190

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