Titlebook: HLA Typing; Methods and Protocol Sebastian Boegel Book 2024Latest edition The Editor(s) (if applicable) and The Author(s), under exclusive

女孩

書(shū)目名稱(chēng)HLA Typing影響因子(影響力)




書(shū)目名稱(chēng)HLA Typing影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)HLA Typing網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)HLA Typing網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)HLA Typing被引頻次




書(shū)目名稱(chēng)HLA Typing被引頻次學(xué)科排名




書(shū)目名稱(chēng)HLA Typing年度引用




書(shū)目名稱(chēng)HLA Typing年度引用學(xué)科排名




書(shū)目名稱(chēng)HLA Typing讀者反饋




書(shū)目名稱(chēng)HLA Typing讀者反饋學(xué)科排名

流動(dòng)性

Allele Frequency Net Database, their corresponding alleles in worldwide human populations. At present, the website contains data from 1784 population samples in more than 14 million individuals from 129 countries on the frequency of genes from different polymorphic regions including data for the human leukocyte antigen (HLA) sys

引水渠

AmpliSAS and AmpliHLA: Web Server and Local Tools for MHC Typing of Non-model Species and Human Usize amplicon sequencing data from non-model species and it is able to perform de novo genotyping without any previous knowledge of the reference alleles. AmpliHLA is a human specific version; it performs HLA typing by comparing sequenced variants against human reference alleles from the IMGT/HLA data

比目魚(yú)

Comprehensive HLA Typing from a Current Allele Database Using Next-Generation Sequencing Data,d inflammation-related disorders, and donor selection in organ transplantation and regenerative medicine. To obtain this information, an accurate . typing method that is applicable for any allele registered in . allele databases is needed. Here we describe a method—called HLA-HD—for determining alle

哀悼

Deep Learning-Based HLA Allele Imputation Applicable to GWAS,genes are identified, to fully understand the genetic basis of human traits. Different HLA imputation methods have been developed, each with its own advantages, and recent methods have been improved in terms of imputation accuracy and computational costs. Here, I describe Deep*HLA, a recently publis

不公開(kāi)

責(zé)怪

Feature

CANON

Imputation-Based HLA Typing with GWAS SNPs, complex (MHC) region. These methods predict HLA classical alleles using dense SNP genotypes, commonly found on array-based platforms used in genome-wide association studies (GWAS). The analysis of HLA classical alleles can be conducted on current SNP datasets at no additional cost. Here, we describ

VALID