SNP array: Difference between revisions

Revision as of 08:44, 19 December 2015

Revision as of 16:10, 29 January 2016

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*{{cite journal |doi=10.1093/dnares/dsm002 |pmid=17363414 |pmc=2779891 |title=Genome-wide Copy Number Profiling on High-density Bacterial Artificial Chromosomes, Single-nucleotide Polymorphisms, and Oligonucleotide Microarrays: A Platform Comparison based on Statistical Power Analysis |journal=DNA Research |volume=14 |issue=1 |pages=1–11 |year=2007 |last1=Hehir-Kwa |first1=J. Y. |last2=Egmont-Petersen |first2=M. |last3=Janssen |first3=I. M. |last4=Smeets |first4=D. |last5=Van Kessel |first5=A. G. |last6=Veltman |first6=J. A. }}

*{{cite journal |doi=10.1086/422195 |pmid=15154113 |pmc=1182008 |title=Whole-Genome Scan, in a Complex Disease, Using 11,245 Single-Nucleotide Polymorphisms: Comparison with Microsatellites |journal=The American Journal of Human Genetics |volume=75 |issue=1 |pages=54–64 |year=2004 |last1=John |first1=Sally |last2=Shephard |first2=Neil |last3=Liu |first3=Guoying |last4=Zeggini |first4=Eleftheria |last5=Cao |first5=Manqiu |last6=Chen |first6=Wenwei |last7=Vasavda |first7=Nisha |last8=Mills |first8=Tracy |last9=Barton |first9=Anne |last10=Hinks |first10=Anne |last11=Eyre |first11=Steve |last12=Jones |first12=Keith W. |last13=Ollier |first13=William |last14=Silman |first14=Alan |last15=Gibson |first15=Neil |last16=Worthington |first16=Jane |last17=Kennedy |first17=Giulia C. }}

*{{cite journal |pmid=10958631 |pmc=2235196 |year=2000 |author1=Mei |first1=R |title=Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays |journal=Genome researchResearch |volume=10 |issue=8 |pages=1126–37 |last2=Galipeau |first2=P. C. |last3=Prass |first3=C |last4=Berno |first4=A |last5=Ghandour |first5=G |last6=Patil |first6=N |last7=Wolff |first7=R. K. |last8=Chee |first8=M. S. |last9=Reid |first9=B. J. |last10=Lockhart |first10=D. J. |doi=10.1101/gr.10.8.1126}}

*{{cite journal |doi=10.1086/425870 |pmid=15514889 |pmc=1182157 |title=Comparison of Microsatellites Versus Single-Nucleotide Polymorphisms in a Genome Linkage Screen for Prostate Cancer–Susceptibility Loci |journal=The American Journal of Human Genetics |volume=75 |issue=6 |pages=948–65 |year=2004 |last1=Schaid |first1=Daniel J. |last2=Guenther |first2=Jennifer C. |last3=Christensen |first3=Gerald B. |last4=Hebbring |first4=Scott |last5=Rosenow |first5=Carsten |last6=Hilker |first6=Christopher A. |last7=McDonnell |first7=Shannon K. |last8=Cunningham |first8=Julie M. |last9=Slager |first9=Susan L. |last10=Blute |first10=Michael L. |last11=Thibodeau |first11=Stephen N. }}

*{{cite journal |doi=10.1093/nar/gnh163 |pmid=15561999 |pmc=534642 |title=Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays |journal=Nucleic Acids Research |volume=32 |issue=20 |pages=e164 |year=2004 |last1=Sellick |first1=G. S. |last2=Longman |first2=C |last3=Tolmie |first3=J |last4=Newbury-Ecob |first4=R |last5=Geenhalgh |first5=L |last6=Hughes |first6=S |last7=Whiteford |first7=M |last8=Garrett |first8=C |last9=Houlston |first9=R. S. }}