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[PDF] Supporting Information for: Inference of population structure using dense haplotype data

[PDF] from bris.ac.ukDJ Lawson, G Hellenthal, S Myers… - 2011 - maths.bris.ac.uk
Page 1. Supporting Information for: Inference of population structure using dense
haplotype data Daniel ... haplotypes. In our no- tation, every individual consists of two
haploids, each consisting of a single phased haplotype per chromosome. ...
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[HTML] The JAK2 46/1 haplotype in splanchnic vein thrombosis

[HTML] from hematologylibrary.orgE Kouroupi, JJ Kiladjian… - …, 2011 - bloodjournal.hematologylibrary.org
We studied this haplotype in a cohort of 170 patients with SVT (sex ratio M/F = 1.12). Approval
was obtained from the PV-Nord Institutional Review Board. Informed consent was obtained in
accordance with the Declaration of Helsinki. As controls we studied 58 non-MPN patients ...
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Data from: Allele mining and phylogenetic analyses of the eIF4E resistance gene in barley reveal exceptionally high sequence and haplotype diversity and a signature …

B Hofinger, J Russell, C Bass, T Baldwin… - 2011 - datadryad.org
In barley the eukaryotic translation initiation factor 4E (eIF4E) gene situated on chromosome
3H is recognised as an important source of resistance to the bymoviruses Barley yellow mosaic
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SNPs and Haplotypes in DPYD and Outcome of Capecitabine–Letter

ABP van Kuilenburg… - Clinical Cancer Research, 2011 - AACR
... A mutation is in cis with a deep intronic mutation c.1129-5923C>G, creating a cryptic splice-donor
site and affecting pre-mRNA splicing (2). In addition, the c.1129-5923C>G splice mutation proved
to be in complete linkage with the previously identified B3 haplotype, which was ...

DASH: A Method for Identical-by-Descent Haplotype Mapping Uncovers Association with Recent Variation.

A Gusev, EE Kenny, JK Lowe, J Salit… - American journal of …, 2011 - ncbi.nlm.nih.gov
Rare variants affecting phenotype pose a unique challenge for human genetics. Although
genome-wide association studies have successfully detected many common causal
variants, they are underpowered in identifying disease variants that are too rare or ...

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