"the number of errors committed by nursing students" trang 8 - tải miễn phí từ tailieunhanh
DBS: A fast and informative segmentation algorithm for DNA copy number analysis

DBS: A fast and informative segmentation algorithm for DNA copy number analysis
14    66    1
DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data
13    38    1
A sparse autoencoder-based deep neural network for protein solvent accessibility and contact number prediction

A sparse autoencoder-based deep neural network for protein solvent accessibility and contact number prediction
10    79    1
Thresher: Determining the number of clusters while removing outliers

Thresher: Determining the number of clusters while removing outliers
15    49    1
Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data

Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data
6    62    1
An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data
13    50    1
SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data

SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data
9    39    1
GenomeCAT: A versatile tool for the analysis and integrative visualization of DNA copy number variants

GenomeCAT: A versatile tool for the analysis and integrative visualization of DNA copy number variants
8    43    1
Identification of recurrent focal copy number variations and their putative targeted driver genes in ovarian cancer

Identification of recurrent focal copy number variations and their putative targeted driver genes in ovarian cancer
12    39    1
CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data
10    99    1
VEGAWES: Variational segmentation on whole exome sequencing for copy number detection

VEGAWES: Variational segmentation on whole exome sequencing for copy number detection
10    51    1
Identification and utilization of copy number information for correcting Hi‑C contact map of cancer cell lines

Identification and utilization of copy number information for correcting Hi‑C contact map of cancer cell lines
25    57    1
Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms

Performance of copy number variants detection based on whole‑genome sequencing by DNBSEQ platforms
14    31    1
BCRgt: A Bayesian cluster regression-based genotyping algorithm for the samples with copy number alterations

BCRgt: A Bayesian cluster regression-based genotyping algorithm for the samples with copy number alterations
12    27    1
A practical approximation algorithm for solving massive instances of hybridization number for binary and nonbinary trees

A practical approximation algorithm for solving massive instances of hybridization number for binary and nonbinary trees
12    33    1
SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations

SubPatCNV: Approximate subspace pattern mining for mapping copy-number variations
12    46    1
SCNVSim: Somatic copy number variation and structure variation simulator

SCNVSim: Somatic copy number variation and structure variation simulator
6    39    1
Not all the number of skeletal muscle fibers is determined prenatally

Not all the number of skeletal muscle fibers is determined prenatally
6    46    1
CNV-TV: A robust method to discover copy number variation from short sequencing reads

CNV-TV: A robust method to discover copy number variation from short sequencing reads
12    42    1
Fast detection of de novo copy number variants from SNP arrays for case-parent trios

Fast detection of de novo copy number variants from SNP arrays for case-parent trios
14    21    1