"high throughput platforms" trang 8 - tải miễn phí từ tailieuXANH
Modeling allele-specific expression at the gene and SNP levels simultaneously by a Bayesian logistic mixed regression model

Modeling allele-specific expression at the gene and SNP levels simultaneously by a Bayesian logistic mixed regression model
13    53    0
Lag penalized weighted correlation for time series clustering

Lag penalized weighted correlation for time series clustering
15    197    0
AnamiR: Integrated analysis of MicroRNA and gene expression profiling

AnamiR: Integrated analysis of MicroRNA and gene expression profiling
7    101    0
NeoPredPipe: High-throughput neoantigen prediction and recognition potential pipeline

NeoPredPipe: High-throughput neoantigen prediction and recognition potential pipeline
6    45    0
Statistical assessment and visualization of synergies for large-scale sparse drug combination datasets

Statistical assessment and visualization of synergies for large-scale sparse drug combination datasets
15    66    0
InTAD: Chromosome conformation guided analysis of enhancer target genes

InTAD: Chromosome conformation guided analysis of enhancer target genes
7    54    0
SLIM: A flexible web application for the reproducible processing of environmental DNA metabarcoding data

SLIM: A flexible web application for the reproducible processing of environmental DNA metabarcoding data
6    48    0
FitTetra 2.0 – improved genotype calling for tetraploids with multiple population and parental data support

FitTetra 2.0 – improved genotype calling for tetraploids with multiple population and parental data support
8    60    0
MS-Helios: A Circos wrapper to visualize multi-omic datasets

MS-Helios: A Circos wrapper to visualize multi-omic datasets
4    62    0
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    50    0
NGmerge: Merging paired-end reads via novel empirically-derived models of sequencing errors

NGmerge: Merging paired-end reads via novel empirically-derived models of sequencing errors
9    63    0
OMeta: An ontology-based, data-driven metadata tracking system

OMeta: An ontology-based, data-driven metadata tracking system
15    51    0
Comparing the performance of selected variant callers using synthetic data and genome segmentation

Comparing the performance of selected variant callers using synthetic data and genome segmentation
11    52    0
VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database

VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database
14    66    0
Semi-supervised machine learning for automated species identification by collagen peptide mass fingerprinting

Semi-supervised machine learning for automated species identification by collagen peptide mass fingerprinting
9    78    0
ToTem: A tool for variant calling pipeline optimization

ToTem: A tool for variant calling pipeline optimization
9    55    0
Benchmarking differential expression analysis tools for RNA-Seq: Normalization-based vs. log-ratio transformation-based methods

Benchmarking differential expression analysis tools for RNA-Seq: Normalization-based vs. log-ratio transformation-based methods
15    71    0
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
6    61    0
Cluster oligonucleotide signatures for rapid identification by sequencing

Cluster oligonucleotide signatures for rapid identification by sequencing
14    47    0
GPrank: An R package for detecting dynamic elements from genome-wide time series

GPrank: An R package for detecting dynamic elements from genome-wide time series
6    51    0
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