"Mutation data" trang 1 - tải miễn phí từ tailieunhanh
MUFFINN: Cancer gene discovery via network analysis of somatic mutation data

MUFFINN: Cancer gene discovery via network analysis of somatic mutation data
16    72    1
Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample

Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer sample
20    40    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    54    1
Mutation status coupled with RNAsequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer

Mutation status coupled with RNAsequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer
11    69    1
Integrating multiple immunogenetic data sources for feature extraction and mining somatic hypermutation patterns: The case of “towards analysis” in chronic lymphocytic leukaemia

Integrating multiple immunogenetic data sources for feature extraction and mining somatic hypermutation patterns: The case of “towards analysis” in chronic lymphocytic leukaemia
13    54    1
GPOPSIM: A simulation tool for whole-genome genetic data

GPOPSIM: A simulation tool for whole-genome genetic data
6    11    1
Báo cáo y học:

Báo cáo y học: " Patient-oriented gene set analysis for cancer mutation data"
10    38    0
Real-world treatment and survival of patients with advanced non-small cell lung Cancer: A German retrospective data analysis

Real-world treatment and survival of patients with advanced non-small cell lung Cancer: A German retrospective data analysis
14    65    0
Cancer prognosis prediction using somatic point mutation and copy number variation data: A comparison of gene‑level and pathway‑based models

Cancer prognosis prediction using somatic point mutation and copy number variation data: A comparison of gene‑level and pathway‑based models
19    61    1
Isma: An R package for the integrative analysis of mutations detected by multiple pipelines

Isma: An R package for the integrative analysis of mutations detected by multiple pipelines
9    84    1
MutScan: Fast detection and visualization of target mutations by scanning FASTQ data

MutScan: Fast detection and visualization of target mutations by scanning FASTQ data
11    76    1
A site specific model and analysis of the neutral somatic mutation rate in whole-genome cancer data

A site specific model and analysis of the neutral somatic mutation rate in whole-genome cancer data
15    60    1
Divisive hierarchical maximum likelihood clustering

Divisive hierarchical maximum likelihood clustering
9    105    3
ISVASE: Identification of sequence variant associated with splicing event using RNAseq data

ISVASE: Identification of sequence variant associated with splicing event using RNAseq data
7    68    1
Gpps: An ILP-based approach for inferring cancer progression with mutation losses from single cell data

Gpps: An ILP-based approach for inferring cancer progression with mutation losses from single cell data
16    38    1
Clinical efficacy comparison of avapritinib with other tyrosine kinase inhibitors in gastrointestinal stromal tumors with PDGF RA D842V mutation: A retrospective analysis of clinical trial and real-world data

Clinical efficacy comparison of avapritinib with other tyrosine kinase inhibitors in gastrointestinal stromal tumors with PDGF RA D842V mutation: A retrospective analysis of clinical trial and real-world data
9    30    1
Osimertinib in advanced EGFRT790M mutation-positive non-small cell lung cancer patients treated within the Special Use Medication Program in Spain: OSIREX-Spanish Lung Cancer Group

Osimertinib in advanced EGFRT790M mutation-positive non-small cell lung cancer patients treated within the Special Use Medication Program in Spain: OSIREX-Spanish Lung Cancer Group
12    32    1
SCReadCounts: Estimation of cell-level SNVs expression from scRNA-seq data

SCReadCounts: Estimation of cell-level SNVs expression from scRNA-seq data
9    25    1
HAPDeNovo: A haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data

HAPDeNovo: A haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data
7    34    1
Analysis of error profiles in deep nextgeneration sequencing data

Analysis of error profiles in deep nextgeneration sequencing data
15    29    1