2015
DOI: 10.1016/j.humimm.2015.06.016
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HLA-E coding and 3′ untranslated region variability determined by next-generation sequencing in two West-African population samples

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Cited by 32 publications
(51 citation statements)
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“…We know that the interaction KIR-HLA has two sides of KIR and HLA. For example overexpression of HLA-E on surface of colorectal cancer cells can result in inhibition of NKs [53] and such patients have better survival from the disease [54]; of course the receptor of HLA-E is CD94/NKG2a [55], [56]. KIR2DL1 and 2DS1 interact with HLA-C2, and KIR2DL2, 2DL3 and 2DS2 interact with HLA-C1 [57]; so every mathematical predict do not occur.…”
Section: Resultsmentioning
confidence: 99%
“…We know that the interaction KIR-HLA has two sides of KIR and HLA. For example overexpression of HLA-E on surface of colorectal cancer cells can result in inhibition of NKs [53] and such patients have better survival from the disease [54]; of course the receptor of HLA-E is CD94/NKG2a [55], [56]. KIR2DL1 and 2DS1 interact with HLA-C2, and KIR2DL2, 2DL3 and 2DS2 interact with HLA-C1 [57]; so every mathematical predict do not occur.…”
Section: Resultsmentioning
confidence: 99%
“…We used VCFx software (Castelli et al. ) to convert our Ensifer genus vcf file of combined E. meliloti and E. medicae SNPs to an aligned fasta file—the input format for ClonalFrame. We performed two runs of ClonalFrame with 100,000 iterations and removed 50,000 as the burn‐in.…”
Section: Methodsmentioning
confidence: 99%
“…We used the program ClonalFrame (Didelot and Falush 2007) to estimate ρ/θ (number of recombination events/number of mutation events). We used VCFx software (Castelli et al 2015) to convert our Ensifer genus vcf file of combined E. meliloti and E. medicae SNPs to an aligned fasta file-the input format for ClonalFrame. We performed two runs of ClonalFrame with 100,000 iterations and removed 50,000 as the burn-in.…”
Section: Structurementioning
confidence: 99%
“…For instance, whole-genome sequencing (WGS) was successfully used to type HLA-A alleles at full resolution in 1070 healthy Japanese individuals [12] and to fully evaluate HLA-E variability in West African populations [13]. However, the main problem with MHC sequencing using current technologies is the relatively short read lengths, which limit the amount of allelic data that can be generated at a high resolution.…”
Section: Advances In Mapping Susceptibility Variants In the Mhc Locusmentioning
confidence: 99%