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deCODE Release 2: whole-genome de novo variants from the proband from 1548 Icelandic trios

NIAID Data Ecosystem2026-03-10 收录

新发变异检测

人类遗传学

数据链接：

https://www.omicsdi.org/dataset/eva/PRJEB21300 数据链接链接失效反馈

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资源简介：

deCODE Release 2: whole-genome de novo variants from the proband from 1548 Icelandic trios

应用场景：

创建时间：

2017-08-10

人类遗传学

基因组分析

The 1000 Genomes Project is an international collaboration which has established the most detailed catalogue of human genetic variation, including SNPs, structural variants, and their haplotype contex

aws亚马逊开源数据集150

Estonian Biocentre Free Data

人类遗传学

基因型数据

A small genotype data repository containing data used in recent papers from the Estonian Biocentre. Most of the data pertains to human population genetics. PDF files of the papers are also freely avai

re3data.org70

Genetic studies of the Seneca Indians: haptoglobins, transferrins, G-6-PD deficiency, hemoglobinopathy, color blindness, morphological traits and dermatoglyphics

人类遗传学

群体遗传学

Genetic studies of the Seneca Indians: haptoglobins, transferrins, G-6-PD deficiency, hemoglobinopathy, color blindness, morphological traits and dermatoglyphics

Global Health Data Exchange ()60

Additional file 1: of Analysis of the human Y-chromosome haplogroup Q characterizes ancient population movements in Eurasia and the Americas

人类遗传学

古代人口迁移

Table S1. List of the high coverage samples analysed in this study along with their geographic origin and Y-chromosome haplogroup affiliation. (XLSX 20 kb)

DataCite Commons2020-08-27 更新120

Additional file 3: Table ST1. of Intricacies in arrangement of SNP haplotypes suggest â Great Admixtureâ that created modern humans

人类遗传学

基因组学

Distribution of CHs has been examined among all human autosomes in 5398 segments, and these data are shown in the Additional file 2: Table ST1. (XLSX 643 kb)

DataCite Commons2024-12-18 更新60

deCODE Release 2: whole-genome de novo variants from the proband from 1548 Icelandic trios

资源简介：

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