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资源简介：
Targeted deep sequencing
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创建时间：
2023-05-23
相关数据集
Additional file 15 of PRINCESS: comprehensive detection of haplotype resolved SNVs, SVs, and methylation
Additional file 15: Table S14. Genotype benchmark percentage using different algorithms.
DataCite Commons2021-09-15 更新100
1137_FCH7L2KCCX2_L5_BISvveXAABBAAA-168_marked_duplicates_NmMdAndUqTag_fixed.vcf-1.gz
:unav
DataCite Commons2024-01-17 更新50
Variants identified by whole genome sequencing for CAT and PCDHB5 loci.
Variants identified by whole genome sequencing for CAT and PCDHB5 loci.
Figshare2023-09-26 更新30
Haemophilus influenzae Rd KW20 Genome sequencing
This study aims to detect rare variations from a single colony by deep sequencing.
NIAID Data Ecosystem60
A Robust GWSS Method to Simultaneously Detect Rare and Common Variants for Complex Disease
The rapid advances in sequencing technologies and the resulting next-generation sequencing data provide the opportunity to detect disease-associated variants with a better solution, in particular for
Figshare2016-01-15 更新30
