genome identification trang 7 tải miễn phí từ TAILIEUCHUNG

"genome identification" trang 7 - tải miễn phí từ Tailieuchung

Systematic identification of intergenic longnoncoding RNAs in mouse retinas using full-length isoform sequencing

Systematic identification of intergenic longnoncoding RNAs in mouse retinas using full-length isoform sequencing

15 18 1

Genomic identification and functional analysis of essential genes in Caenorhabditis elegans

Genomic identification and functional analysis of essential genes in Caenorhabditis elegans

14 10 1

Global identification and characterization of lncRNAs that control inflammation in malignant cholangiocytes

Global identification and characterization of lncRNAs that control inflammation in malignant cholangiocytes

13 15 1

Comprehensive genome-wide analysis of calmodulin-binding transcription activator (CAMTA) in Durio zibethinus and identification of fruit ripening-associated DzCAMTAs

Comprehensive genome-wide analysis of calmodulin-binding transcription activator (CAMTA) in Durio zibethinus and identification of fruit ripening-associated DzCAMTAs

22 22 1

Computational identification of harmful mutation regions to the activity of transposable elements

Computational identification of harmful mutation regions to the activity of transposable elements

15 46 1

Genome-wide identification of Chiari malformation type I associated candidate genes and chromosomal variations

Genome-wide identification of Chiari malformation type I associated candidate genes and chromosomal variations

13 25 1

CCMetagen: Comprehensive and accurate identification of eukaryotes and prokaryotes in metagenomic data

CCMetagen: Comprehensive and accurate identification of eukaryotes and prokaryotes in metagenomic data

15 38 1

HBA-DEALS: Accurate and simultaneous identification of differential expression and splicing using hierarchical Bayesian analysis

HBA-DEALS: Accurate and simultaneous identification of differential expression and splicing using hierarchical Bayesian analysis

20 14 1

BRIE2: Computational identification of splicing phenotypes from single-cell transcriptomic experiments

BRIE2: Computational identification of splicing phenotypes from single-cell transcriptomic experiments

15 36 1

Evaluation of some aspects in supervised cell type identification for single-cell RNAseq: Classifier, feature selection, and reference construction

Evaluation of some aspects in supervised cell type identification for single-cell RNAseq: Classifier, feature selection, and reference construction

23 15 1

An explainable artificial intelligence approach for decoding the enhancer histone modifications code and identification of novel enhancers in Drosophila

An explainable artificial intelligence approach for decoding the enhancer histone modifications code and identification of novel enhancers in Drosophila

23 43 1

A cis-regulatory-directed pipeline for the identification of genes involved in cardiac development and disease

A cis-regulatory-directed pipeline for the identification of genes involved in cardiac development and disease

21 12 1

STARRPeaker: Uniform processing and accurate identification of STARR-seq active regions

STARRPeaker: Uniform processing and accurate identification of STARR-seq active regions

24 14 1

Comprehensive identification of somatic nucleotide variants in human brain tissue

Comprehensive identification of somatic nucleotide variants in human brain tissue

32 39 1

A survey of best practices for RNA-seq data analysis

A survey of best practices for RNA-seq data analysis

19 18 1

Systematic identification of genetic influences on methylation across the human life course

Systematic identification of genetic influences on methylation across the human life course

14 47 1

DESMAN: A new tool for de novo extraction of strains from metagenomes

DESMAN: A new tool for de novo extraction of strains from metagenomes

22 37 1

Systematic identification of regulatory variants associated with cancer risk

Systematic identification of regulatory variants associated with cancer risk

14 39 1

OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps

OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps

19 10 3

DIVAN: Accurate identification of noncoding disease-specific risk variants using multi-omics profiles

DIVAN: Accurate identification of noncoding disease-specific risk variants using multi-omics profiles

21 39 3

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