"sequencing simulator" trang 6 - tải miễn phí từ tailieunhanh
Depletion of Abundant Sequences by Hybridization (DASH): Using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications

Depletion of Abundant Sequences by Hybridization (DASH): Using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications
13    14    1
Streamlined analysis of duplex sequencing data with Du Novo

Streamlined analysis of duplex sequencing data with Du Novo
10    250    1
Characterization of background noise in capture-based targeted sequencing data

Characterization of background noise in capture-based targeted sequencing data
13    51    1
Evaluating nanopore sequencing data processing pipelines for structural variation identification

Evaluating nanopore sequencing data processing pipelines for structural variation identification
13    64    3
Analysis of error profiles in deep nextgeneration sequencing data

Analysis of error profiles in deep nextgeneration sequencing data
15    29    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    28    1
Performance of neural network basecalling tools for Oxford Nanopore sequencing

Performance of neural network basecalling tools for Oxford Nanopore sequencing
10    13    1
Decreasing miRNA sequencing bias using a single adapter and circularization approach

Decreasing miRNA sequencing bias using a single adapter and circularization approach
9    23    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    22    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    20    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    11    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    10    1
Ebook Principles of Sequencing and Scheduling: Part 2

Ebook Principles of Sequencing and Scheduling: Part 2
295    12    1
Beyond the exome: Utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases

Beyond the exome: Utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases
16    11    1
Rare subclonal sequencing of breast cancers indicates putative metastatic driver mutations are predominately acquired after dissemination

Rare subclonal sequencing of breast cancers indicates putative metastatic driver mutations are predominately acquired after dissemination
19    16    1
Improved genome sequencing using an engineered transposase

Improved genome sequencing using an engineered transposase
10    64    1
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    62    1
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    75    1
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    51    1