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                             14 results found
no title author magazine year volume issue page(s) type
1 A comparative analysis of exome capture Parla, Jennifer S
2011
12 9 article
2 Comparison of solution-based exome capture methods for next generation sequencing Sulonen, Anna-Maija
2011
12 9 article
3 Comprehensive comparison of three commercial human whole-exome capture platforms Asan,
2011
12 9 article
4 Effective detection of rare variants in pooled DNA samples using Cross-pool tailcurve analysis Niranjan, Tejasvi S
2011
12 9 article
5 Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice Hilton, Jennifer M
2011
12 9 article
6 Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia Takata, Atsushi
2011
12 9 article
7 Expanding whole exome resequencing into non-human primates Vallender, Eric J
2011
12 9 article
8 First somatic mutation of E2F1 in a critical DNA binding residue discovered in well-differentiated papillary mesothelioma of the peritoneum Yu, Willie
2011
12 9 article
9 Mutation discovery in mice by whole exome sequencing Fairfield, Heather
2011
12 9 article
10 Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes Smith, Katherine R
2011
12 9 article
11 SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing Tariq, Muhammad
2011
12 9 article
12 Targeted analysis of nucleotide and copy number variation by exon capture in allotetraploid wheat genome Saintenac, Cyrille
2011
12 9 article
13 Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families Brownstein, Zippora
2011
12 9 article
14 The functional spectrum of low-frequency coding variation Marth, Gabor T
2011
12 9 article
                             14 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands