"sequencing simulator" trang 6 - tải miễn phí từ tailieuXANH
Streamlined analysis of duplex sequencing data with Du Novo

Streamlined analysis of duplex sequencing data with Du Novo
10    25    1
Characterization of background noise in capture-based targeted sequencing data

Characterization of background noise in capture-based targeted sequencing data
13    29    1
Evaluating nanopore sequencing data processing pipelines for structural variation identification

Evaluating nanopore sequencing data processing pipelines for structural variation identification
13    64    2
Analysis of error profiles in deep nextgeneration sequencing data

Analysis of error profiles in deep nextgeneration sequencing data
15    17    1
Measuring sequencer size bias using REcount: A novel method for highly accurate Illumina sequencing-based quantification

Measuring sequencer size bias using REcount: A novel method for highly accurate Illumina sequencing-based quantification
17    16    1
Performance of neural network basecalling tools for Oxford Nanopore sequencing

Performance of neural network basecalling tools for Oxford Nanopore sequencing
10    14    1
Decreasing miRNA sequencing bias using a single adapter and circularization approach

Decreasing miRNA sequencing bias using a single adapter and circularization approach
9    21    1
PHLI-seq: Constructing and visualizing cancer genomic maps in 3D by phenotypebased high-throughput laser-aided isolation and sequencing

PHLI-seq: Constructing and visualizing cancer genomic maps in 3D by phenotypebased high-throughput laser-aided isolation and sequencing
17    8    1
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
Identification of single nucleotide variants in the Moroccan population by wholegenome sequencing

Identification of single nucleotide variants in the Moroccan population by wholegenome sequencing
8    8    1
Exome sequencing in one family with gastric- and rectal cancer

Exome sequencing in one family with gastric- and rectal cancer
8    2    1
Combined small RNA and degradome sequencing to identify miRNAs and their targets in response to drought in foxtail millet

Combined small RNA and degradome sequencing to identify miRNAs and their targets in response to drought in foxtail millet
16    2    1
Improved genome sequencing using an engineered transposase

Improved genome sequencing using an engineered transposase
10    144    2
Optimized sequencing depth and de novo assembler for deeply reconstructing the transcriptome of the tea plant, an economically important plant species

Optimized sequencing depth and de novo assembler for deeply reconstructing the transcriptome of the tea plant, an economically important plant species
11    52    0
HGT-ID: An efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data

HGT-ID: An efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data
11    71    0
Fast-GBS: A new pipeline for the efficient and highly accurate calling of SNPs from genotyping-by-sequencing data

Fast-GBS: A new pipeline for the efficient and highly accurate calling of SNPs from genotyping-by-sequencing data
7    76    0
Rapid evaluation and quality control of next generation sequencing data with FaQCs

Rapid evaluation and quality control of next generation sequencing data with FaQCs
8    74    0
ANGSD: Analysis of next generation sequencing data

ANGSD: Analysis of next generation sequencing data
13    56    0
Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing

Snp-search: Simple processing, manipulation and searching of SNPs from high-throughput sequencing
8    53    0
Adaptation of Oxford Nanopore technology for hepatitis C whole genome sequencing and identification of within-host viral variants

Adaptation of Oxford Nanopore technology for hepatitis C whole genome sequencing and identification of within-host viral variants
12    32    1
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