Objective: Our goal was to evaluate the influence of quality control (QC) decisions using two genotype calling algorithms, CRLMM and Birdseed, designed for the Affymetrix SNP Array 6.0. Methods: ...
Single nucleotide polymorphisms (SNPs) are sequence variants in which two alternate bases occur at one position. The SNP Consortium is developing a dense map of SNPs in the hope that certain variants ...
In 467 consecutive patients with ALL (0-20 years), we compared RNA sequencing (RNAseq), fluorescence in situ hybridization (FISH), reverse transcriptase polymerase chain reaction (RT-PCR), karyotyping ...
PAM50 intrinsic subtyping and pathologic responses to neoadjuvant trastuzumab-based chemotherapy in HER2-positive breast cancer. Background: Early detection and monitoring the progress of common ...
In 2011 genomic selection (GS) was implemented in Swiss cattle and large-scale genotyping data became available. This significant change enables now a comparative approach between identification of ...
Using SNP-CGH to Profile for Amplifications, Duplications, and Deletions The beginnings of personalized medicine have been forged by recent advances in SNP genotyping technologies. It is now possible ...
Using the information in the HapMap, researchers are able to find genes that affect health, disease, and individual responses to medications and environmental factors. For example, the goal of the ...
We conducted a study to show that we can accurately discriminate embryos that carry a BCR from those that do not, as well as detect the presence of cryptic imbalances and complex rearrangements, using ...
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