microarray snp genotype data (Illumina Inc)
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Illumina Inc
microarray snp genotype data
Microarray Snp Genotype Data, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/snp+microarray+data/snp+genotypes/pm40563917-118-13-18
Average 90 stars, based on 1 article reviews
Microarray Snp Genotype Data, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/snp+microarray+data/snp+genotypes/pm40563917-118-13-18
Average 90 stars, based on 1 article reviews
microarray snp genotype data - by Bioz Stars,
2026-09
90/100 stars
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Microarray:Article Title: Excess of rare, inherited truncating mutations in autism Article Snippet: .. In addition, we compared SNPs from exome calls with SNP calls from existing Article Title: Excess of rare, inherited truncating mutations in autism Article Snippet: .. In addition, we compared SNPs from exome calls with SNP calls from existing Illumina Article Title: Excess of rare, inherited truncating mutations in autism Article Snippet: .. Finally, to ensure we did not have any sample, family or data mix-ups, we used a custom-developed (Sanders, personal communication) tool to identify and match 287 polymorphic SNPs in each exome to an existing database of “SNP fingerprints” derived from Article Title: The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing. Article Snippet: .. Comparison to SNP microarray genotype data SNP genotypes were available for more than 4 million loci for the parents of the trio, NA12889 and NA12890, based on a set of Article Title: De novo rates and selection of large copy number variation Article Snippet: Illumina Hap550 genotyping data used for this purpose consisted of lymphoblastoid cell line DNA from 671 neurologically normal Caucasian controls from a study of Parkinson's disease (dbGaP accession no. phs000089; Simon-Sanchez et al. 2007 ) and peripheral blood DNA from 699 individuals of European ancestry from the InCHIANTI study of aging ( http://www.inchiantistudy.net ; Melzer et al. 2008 ). .. CNV discovery Discovery of de novo CNVs was carried out as an extension of a previously validated method that identifies CNVs from Article Title: The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing Article Snippet: .. SNP genotypes were available for more than 4 million loci for the parents of the trio, NA12889 and NA12890, based on a set of Derivative Assay:Article Title: Excess of rare, inherited truncating mutations in autism Article Snippet: .. Finally, to ensure we did not have any sample, family or data mix-ups, we used a custom-developed (Sanders, personal communication) tool to identify and match 287 polymorphic SNPs in each exome to an existing database of “SNP fingerprints” derived from Comparison:Article Title: The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing. Article Snippet: .. Comparison to SNP microarray genotype data SNP genotypes were available for more than 4 million loci for the parents of the trio, NA12889 and NA12890, based on a set of Generated:Article Title: The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing. Article Snippet: .. Comparison to SNP microarray genotype data SNP genotypes were available for more than 4 million loci for the parents of the trio, NA12889 and NA12890, based on a set of Article Title: The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing Article Snippet: .. SNP genotypes were available for more than 4 million loci for the parents of the trio, NA12889 and NA12890, based on a set of |
