SNPs included in commercial personal genomic testing panels for cancer risk assessment in July 2012. Table S2. Distribution of genetic risk estimates returned to 23andMe customers in the PGen Study. Table S3. Distribution of genetic risk estimates returned to Pathway Genomics customers in the PGen Study. Table S4. Sensitivity analyses: characterization of the outcome. Table S5. Sensitivity analyses: characterization of genetic risk results. Table S6. Sensitivity analyses: screening behaviors and missing data. (PDF 461Â kb
Table S1. Results from the stepwise variable selection method using multivariable mixture cure model...
Table S1. Demographic and Clinical Features and BRCA1/2 testing rationale, Table S2. Reasons why BRC...
Additional file 1: Table S1 Participating samples and their origin sites in the ILCCO lung cancer On...
Table S1. Comprehensive list of single nucleotide polymorphisms (herein called genetic variants) and...
Participant characteristics including age, marital status, education, and number of relatives with P...
Table S1. contains the list of the genes used in the study, as well as indicators for which pathway ...
Table S1. 48 genes included in the TruSeq Amplicon Cancer Panel (TSACP, Illumina), which includes 21...
Phenotypes and covariates. Table S2. Phenotype heritability. Table S3. Lambdas for all traits, calcu...
Table S1. Overview of projects in the PeopleSeq Consortium included in this analysis. Table S2. Stud...
Table S1. Growth media for breast cancer cell lines used in study. Table S2. PTEN protein abundance ...
Additional file 1: Table S1. The UKB data-field ID for each phenotype used in this study. Table S2. ...
Figure S1. Quality assessment of the seven patient cohorts used in this study. Figure S2. Percentage...
Table S1. Drug classes in DEPO (database of evidence for precision oncology). Table S2. Sensitive dr...
Additional file 1: Table S1. Cancer Site Coding Following SEER and WHO Guidelines. Table S2. Unique ...
Table S1. All single nucleotide variants in the NOD2 gene used in GenePy validation. Figure S1. Medi...
Table S1. Results from the stepwise variable selection method using multivariable mixture cure model...
Table S1. Demographic and Clinical Features and BRCA1/2 testing rationale, Table S2. Reasons why BRC...
Additional file 1: Table S1 Participating samples and their origin sites in the ILCCO lung cancer On...
Table S1. Comprehensive list of single nucleotide polymorphisms (herein called genetic variants) and...
Participant characteristics including age, marital status, education, and number of relatives with P...
Table S1. contains the list of the genes used in the study, as well as indicators for which pathway ...
Table S1. 48 genes included in the TruSeq Amplicon Cancer Panel (TSACP, Illumina), which includes 21...
Phenotypes and covariates. Table S2. Phenotype heritability. Table S3. Lambdas for all traits, calcu...
Table S1. Overview of projects in the PeopleSeq Consortium included in this analysis. Table S2. Stud...
Table S1. Growth media for breast cancer cell lines used in study. Table S2. PTEN protein abundance ...
Additional file 1: Table S1. The UKB data-field ID for each phenotype used in this study. Table S2. ...
Figure S1. Quality assessment of the seven patient cohorts used in this study. Figure S2. Percentage...
Table S1. Drug classes in DEPO (database of evidence for precision oncology). Table S2. Sensitive dr...
Additional file 1: Table S1. Cancer Site Coding Following SEER and WHO Guidelines. Table S2. Unique ...
Table S1. All single nucleotide variants in the NOD2 gene used in GenePy validation. Figure S1. Medi...
Table S1. Results from the stepwise variable selection method using multivariable mixture cure model...
Table S1. Demographic and Clinical Features and BRCA1/2 testing rationale, Table S2. Reasons why BRC...
Additional file 1: Table S1 Participating samples and their origin sites in the ILCCO lung cancer On...