Pages that link to "Q37140342"

The following pages link to A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods (Q37140342):

Displaying 24 items.

• arrayMap: a reference resource for genomic copy number imbalances in human malignancies (Q21134582) (← links)
• The pitfalls of platform comparison: DNA copy number array technologies assessed (Q30967336) (← links)
• TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays (Q33576281) (← links)
• Joint estimation of DNA copy number from multiple platforms (Q33779649) (← links)
• A novel SNP analysis method to detect copy number alterations with an unbiased reference signal directly from tumor samples (Q33804466) (← links)
• A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. (Q33892998) (← links)
• Transcriptional profile of tuberculosis antigen-specific T cells reveals novel multifunctional features (Q34146397) (← links)
• Characterization of colon cancer cells: a functional approach characterizing CD133 as a potential stem cell marker (Q34203737) (← links)
• Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus (Q34212342) (← links)
• Visualization of genomic changes by segmented smoothing using an L0 penalty (Q34297079) (← links)
• Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort (Q34306097) (← links)
• Integrative genome-wide expression profiling identifies three distinct molecular subgroups of renal cell carcinoma with different patient outcome (Q34348285) (← links)
• Simple binary segmentation frameworks for identifying variation in DNA copy number (Q34459632) (← links)
• Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing (Q34474098) (← links)
• Suppression of lung adenocarcinoma progression by Nkx2-1 (Q34939788) (← links)
• Tolerance of whole-genome doubling propagates chromosomal instability and accelerates cancer genome evolution. (Q34946877) (← links)
• Parent-specific copy number in paired tumor-normal studies using circular binary segmentation (Q35107920) (← links)
• Alterations of LKB1 and KRAS and risk of brain metastasis: comprehensive characterization by mutation analysis, copy number, and gene expression in non-small-cell lung carcinoma. (Q35185119) (← links)
• Improved multiplex ligation-dependent probe amplification analysis identifies a deleterious PMS2 allele generated by recombination with crossover between PMS2 and PMS2CL. (Q36098562) (← links)
• An integrated systems biology approach identifies positive cofactor 4 as a factor that increases reprogramming efficiency (Q36588918) (← links)
• A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6. (Q37324776) (← links)
• Preprocessing and downstream analysis of microarray DNA copy number profiles (Q37695981) (← links)
• Tumor Evolution of Glioma-Intrinsic Gene Expression Subtypes Associates with Immunological Changes in the Microenvironment. (Q46410671) (← links)
• Henrik Bengtsson (Q89394352) (← links)