next generation sequencing trang 12 tải miễn phí từ TAILIEUCHUNG

"next generation sequencing" trang 12 - tải miễn phí từ Tailieuchung

High-sensitivity HLA typing by Saturated Tiling Capture Sequencing (STC-Seq)

High-sensitivity HLA typing by Saturated Tiling Capture Sequencing (STC-Seq)

10 49 1

MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data

MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data

11 44 1

Báo cáo y học: "Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcript"

1 34 0

Báo cáo y học: "Genomics through the lens of next-generation sequencing"

1 39 0

Báo cáo y học: "Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA"

12 30 0

Báo cáo y học: "Comparison of solution-based exome capture methods for next generation sequencing"

18 27 0

Báo cáo y học: "High-throughput RNA interference screening using pooled shRNA libraries and next generation sequencing"

41 27 0

báo cáo khoa học:

báo cáo khoa học: " Overcoming bias and systematic errors in next generation sequencing data"

5 68 0

Plant microRNAs: New players in functional genomics

Plant microRNAs: New players in functional genomics

21 76 0

Mining cytochrome P450 genes through next generation sequencing and metagenomic analysis from Binh Chau hot spring

Mining cytochrome P450 genes through next generation sequencing and metagenomic analysis from Binh Chau hot spring

5 76 0

Trends and methodologies of bioinformatics: Part 2

Trends and methodologies of bioinformatics: Part 2

436 73 0

Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children – a case report with a review

Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children – a case report with a review

7 49 0

Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children

Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children

7 39 0

Atypical CHARGE associated with a novel frameshift mutation of CHD7 in a Chinese neonatal patient

Atypical CHARGE associated with a novel frameshift mutation of CHD7 in a Chinese neonatal patient

6 95 0

A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: A case report

A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: A case report

6 76 0

Genetic and clinical characteristics of Chinese children with Glucokinasematurity-onset diabetes of the young (GCKMODY)

Genetic and clinical characteristics of Chinese children with Glucokinasematurity-onset diabetes of the young (GCKMODY)

8 81 0

Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: A case report

Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: A case report

7 32 0

Salivary miRNA profiles identify children with autism spectrum disorder, correlate with adaptive behavior, and implicate ASD candidate genes involved in neurodevelopment

Salivary miRNA profiles identify children with autism spectrum disorder, correlate with adaptive behavior, and implicate ASD candidate genes involved in neurodevelopment

11 41 0

Ligation-anchored PCR unveils immune repertoire of TCR-beta from whole blood

Ligation-anchored PCR unveils immune repertoire of TCR-beta from whole blood

10 92 0

Transcriptome profiling and environmental linkage to salinity across Salicornia europaea vegetation

Transcriptome profiling and environmental linkage to salinity across Salicornia europaea vegetation

14 47 0

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