"exome sequencing" trang 3 - tải miễn phí từ tailieuXANH
A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing

A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing
10    7    1
Impact of post-alignment processing in variant discovery from whole exome data

Impact of post-alignment processing in variant discovery from whole exome data
13    68    0
Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data

Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data
8    190    1
Identification of candidate cancer predisposing variants by performing wholeexome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families

Identification of candidate cancer predisposing variants by performing wholeexome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families
11    70    0
Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis

Clinical application of genomic profiling to find druggable targets for adolescent and young adult (AYA) cancer patients with metastasis
10    72    0
Whole exome sequencing of microdissected splenic marginal zone lymphoma: A study to discover novel tumor-specific mutations

Whole exome sequencing of microdissected splenic marginal zone lymphoma: A study to discover novel tumor-specific mutations
10    88    0
Determining the origin of synchronous multifocal bladder cancer by exome sequencing

Determining the origin of synchronous multifocal bladder cancer by exome sequencing
7    65    0
Tumor evolution and intratumor heterogeneity of an epithelial ovarian cancer investigated using next-generation sequencing

Tumor evolution and intratumor heterogeneity of an epithelial ovarian cancer investigated using next-generation sequencing
9    64    0
GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases

GenIO: A phenotype-genotype analysis web server for clinical genomics of rare diseases
6    49    0
Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data

Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data
9    82    0
Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants

Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants
9    31    1
PaCBAM: Fast and scalable processing of whole exome and targeted sequencing data

PaCBAM: Fast and scalable processing of whole exome and targeted sequencing data
5    223    2
Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis

Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis
13    150    1
Dynamic alterations of genome and transcriptome in KRAS G13D mutant CRC PDX model treated with cetuximab

Dynamic alterations of genome and transcriptome in KRAS G13D mutant CRC PDX model treated with cetuximab
10    63    0
Detection of internal exon deletion with exon Del

Detection of internal exon deletion with exon Del
6    107    0
Báo cáo y học:

Báo cáo y học: "eening the human exome: a comparison of whole genome and whole transcriptome sequencing"
1    67    0
Báo cáo y học:

Báo cáo y học: "Exome sequencing: the expert view"
3    58    0
Báo cáo y học:

Báo cáo y học: " Computational and statistical approaches to analyzing variants identified by exome sequencing"
10    48    0
Báo cáo y học:

Báo cáo y học: ": Unlocking Mendelian disease using exome sequencing"
11    46    0
Báo cáo y học:

Báo cáo y học: "Mutation discovery in mice by whole exome sequencing"
12    54    0
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