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资源简介：
whole genome sequencing of 166 MA lines in 7 environments.
应用场景：
创建时间：
2018-12-17
相关数据集
Number of events and rates (plus 95% confidence intervals [CI]) of gain and loss (per copy per generation) for each TE superfamily in which events were observed averaged across all MA lines.
Gains and losses based on whole genome sequence data from Daphnia magna mutation accumulation lines descended from 9 starting genotypes collected from Finland, Germany, and Israel.
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Clinical exome sequencing for Autosomal recessive bestrophinopathy
Clinical exome sequencing results associated with a novel compound heterozygous mutation of the BEST1 gene in two siblings with autosomal recessive bestrophinopathy
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JAAD-D-19-02716 Supplemental materials
Supplementary materials for publication JAAD-D-19-02716 (Lim et al. Novel Mutations Identified by Whole Exome Sequencing in Acral Melanoma. J Am Acad Dermatol. 2020) Supplementary Appendix 1: Detailed
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Mutations in glpT of ten randomly chosen spontaneous mutants of P. aeruginosa PA14 selected from in vitro and in vivo experiments.
Mutants were arranged according to the nucleotide position using the A of the ATG of the ORF as reference.
Figshare2015-12-02 更新40
National Cancer Institute Cancer Genome Characterization Initiative (CGCI)
The Office of Cancer Genomics at the National Cancer Institute sponsored a series of studies as part of the Cancer Genome Characterization Initiative (CGCI) to assess novel emerging sequencing technol
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