Coloboma.003 通过CA/NGS技术识别的各种连锁区域中的SNP、微插入缺失和序列间隙：数量与基因组位置

资源简介

Coloboma.003 通过CA/NGS技术识别的各种连锁区域中的SNP、微插入缺失和序列间隙：数量与基因组位置

【数据集背景】

本数据集源站标题为《Coloboma.003 SNPs, micro-indels, and sequence gaps identified in the various linked regions using CA/NGS technology: Number and genomic location.》。配套论文《Defining the Sequence Elements and Candidate Genes for the Coloboma Mutation》发表于 PLoS ONE（2013），DOI：10.1371/journal.pone.0060267。源站首次发布：2013-04-09。

【数据内容】

源站原始描述：AThe original number of variants identified after bioinformatics analyses, prior to multiple pairwise-line comparisons to identify unique variants. BUnique variants are those specific to Co.003 only after multiple pairwise-line genomic comparisons. See Methods for details as to unique variant identification. Note: Shared variants were ruled out as causative towards the coloboma mutation and submitted to NCBI (Accession No. ss472340674–ss472343089). CCR = causative region. 990,268 bp is the CR id…

【数据结构与技术规格】

文件数 1 个，合计 5.63 KB。Table_2.xls：application/vnd.ms-excel，5.63 KB。数据集 DOI：10.1371/journal.pone.0060267.t002。

【主题与分类】

源站学科分类：Biological Sciences。主题标签：developmental biology、morphogenesis、Birth defects、Limb development、Organism development、Pattern formation、Teratology、Cell differentiation、embryology、genetics。

【适用方向】

源站学科分类标注为 Biological Sciences。

【获取与许可】

源站页面：https://plos.figshare.com/articles/dataset/_Coloboma_003_SNPs_micro_indels_and_sequence_gaps_identified_in_the_various_linked_regions_using_CA_NGS_technology_Number_and_genomic_location_/679019

使用许可：CC BY 4.0（https://creativecommons.org/licenses/by/4.0/）。

规范引用：A. Robb, Elizabeth; B. Antin, Parker; E. Delany, Mary (2015). Coloboma.003 SNPs, micro-indels, and sequence gaps identified in the various linked regions using CA/NGS technology: Number and genomic location.. PLOS ONE. Dataset

【使用注意】

· 源站最后修改于 2023-06-09，引用时请注意版本时效。