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whole-exome sequencing revealed the intratumoral genetic heterogeneity of HCC
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2016-11-02
相关数据集
Additional file 1: of Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients
Clinical characteristics and WES results (including evidence of pathogenicity according to ACMG criteria) of 85 patients studied. (XLSX 24 kb)
Figshare2018-11-08 更新50
Additional file 1: Table S1. of Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese
Detailed information of samples. Table S2. Analysis of rare coding variants. Table S3. Description and summary of quality control steps of whole-exome sequencing samples. Table S4. Exome sequencing co
NIAID Data Ecosystem50
In situ tumor arrays reveal early environmental control of cancer immunity [Whole Exome Sequencing]
We use a laser to implant tumor cells in a regular pattern on the ears of the animal. When GFP expressing tumor cells are implanted in a CD4-Cre Tdtomato mouse we can perform live imaging of red T Cel
NIAID Data Ecosystem40
Additional file 1: of Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder
List of ID/ASD genes. (XLSX 23 kb)
NIAID Data Ecosystem50
Table_1_Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.DOCX
Pathogenic variants in known breast cancer (BC) predisposing genes explain only about 30% of Hereditary Breast Cancer (HBC) cases, whereas the underlying genetic factors for most families remain unkno
NIAID Data Ecosystem40
