"nucleotide sequencing" trang 3 - tải miễn phí từ tailieunhanh
Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness – a case report for dual diagnosis

Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness – a case report for dual diagnosis
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Genome-wide association study identified candidate genes controlling continuous storage root formation and bulking in hexaploid sweetpotato

Genome-wide association study identified candidate genes controlling continuous storage root formation and bulking in hexaploid sweetpotato
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A high-density genetic map constructed using specific length amplified fragment (SLAF) sequencing and QTL mapping of seed-related traits in sesame (Sesamum indicum L.)

A high-density genetic map constructed using specific length amplified fragment (SLAF) sequencing and QTL mapping of seed-related traits in sesame (Sesamum indicum L.)
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ddRAD sequencing-based identification of inter-genepool SNPs and association analysis in Brassica juncea

ddRAD sequencing-based identification of inter-genepool SNPs and association analysis in Brassica juncea
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Comprehensive mutation detection of BRCA1/2 genes reveals large genomic rearrangements contribute to hereditary breast and ovarian cancer in Chinese women

Comprehensive mutation detection of BRCA1/2 genes reveals large genomic rearrangements contribute to hereditary breast and ovarian cancer in Chinese women
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Genome-wide association studies of seven agronomic traits under two sowing conditions in bread wheat

Genome-wide association studies of seven agronomic traits under two sowing conditions in bread wheat
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First insight into the somatic mutation burden of neurofibromatosis type 2- associated grade I and grade II meningiomas: A case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation

First insight into the somatic mutation burden of neurofibromatosis type 2- associated grade I and grade II meningiomas: A case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation
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Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma

Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma
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Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads

Sensitive detection of circular DNAs at single-nucleotide resolution using guided realignment of partially aligned reads
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Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites

Variant site strain typer (VaST): Efficient strain typing using a minimal number of variant genomic sites
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BARCOSEL: A tool for selecting an optimal barcode set for high-throughput sequencing

BARCOSEL: A tool for selecting an optimal barcode set for high-throughput sequencing
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Valection: Design optimization for validation and verification studies

Valection: Design optimization for validation and verification studies
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Germline contamination and leakage in whole genome somatic single nucleotide variant detection

Germline contamination and leakage in whole genome somatic single nucleotide variant detection
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Canary: An atomic pipeline for clinical amplicon assays

Canary: An atomic pipeline for clinical amplicon assays
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Correcting nucleotide-specific biases in high-throughput sequencing data

Correcting nucleotide-specific biases in high-throughput sequencing data
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Whole genome SNP genotype piecemeal imputation

Whole genome SNP genotype piecemeal imputation
11    47    1
NucAmino: A nucleotide to amino acid alignment optimized for virus gene sequences

NucAmino: A nucleotide to amino acid alignment optimized for virus gene sequences
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PGen: Large-scale genomic variations analysis workflow and browser in SoyKB

PGen: Large-scale genomic variations analysis workflow and browser in SoyKB
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Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data

Afull Bayesian partitionmodelfor identifying hypo- and hyper-methylated loci from single nucleotide resolution sequencing data
13    43    1
Using expected sequence features to improve basecalling accuracy of amplicon pyrosequencing data

Using expected sequence features to improve basecalling accuracy of amplicon pyrosequencing data
10    43    1