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Comparative analysis of novel MGISEQ-2000 sequencing platform vs Illumina HiSeq 2500 for whole-genome sequencing

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全基因组测序平台比较

基因测序性能评估

数据链接：

https://www.ncbi.nlm.nih.gov/sra/SRP190016 数据链接链接失效反馈

官方服务：

资源简介：

Full description is published on biorxiv (see links)

应用场景：

创建时间：

2019-04-02

基因测序性能评估

EGFR突变研究

*Calculated for 1,000,000 copies of a 225 bp segment taken from exon 20 of the human EGFR gene (see Exon 20 reference sequence in Supplementary Materials S1). Simple mutations are randomly placed sing

Figshare2015-12-02 更新30

Performance of Illumina and 454 sequencing for the detection of amino acid minority variants within the control library.

基因测序性能评估

变异检测

Expected variant percentages include positions where a MV is present on more than one clone. Median variant % reflects only the minority variants detected by each platform and does not include the und

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Summary statistics characterizing the performance of multiple sequencing runs in recovering a core set of loci.

基因测序性能评估

核心位点恢复

Analysis based on a set of 5,996 loci genotyped in all 46 samples in RAD10 with per locus sequencing depth ≥5 reads for all 46 samples.Summary statistics characterizing the performance of multiple seq

Figshare2015-12-02 更新00

Coverage Bias and Sensitivity of Variant Calling for Four Whole-genome Sequencing Technologies

全基因组测序平台比较

变异检出评估

The emergence of high-throughput, next-generation sequencing technologies has dramatically altered the way we assess genomes in population genetics and in cancer genomics. Currently, there are four co

Figshare2016-01-18 更新30

Sensitivity and specificity over three mock sequencing runs.

基因测序性能评估

诊断分析

Values are reported as mean (standard deviation).

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