"Sequencing errors" trang 1 - tải miễn phí từ tailieunhanh
PaSS: A sequencing simulator for PacBio sequencing

PaSS: A sequencing simulator for PacBio sequencing
7    65    1
SMOOTH-seq: Single-cell genome sequencing of human cells on a thirdgeneration sequencing platform

SMOOTH-seq: Single-cell genome sequencing of human cells on a thirdgeneration sequencing platform
19    52    1
The applications of massive parallel sequencing (next-generation sequencing) in research and molecular diagnosis of human genetic diseases

The applications of massive parallel sequencing (next-generation sequencing) in research and molecular diagnosis of human genetic diseases
14    94    0
Optimal sequencing depth design for whole genome re-sequencing in pigs

Optimal sequencing depth design for whole genome re-sequencing in pigs
12    53    1
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    1
CarrierSeq: A sequence analysis workflow for low-input nanopore sequencing

CarrierSeq: A sequence analysis workflow for low-input nanopore sequencing
4    60    1
Comparing variant calling algorithms for target-exon sequencing in a large sample

Comparing variant calling algorithms for target-exon sequencing in a large sample
10    45    1
Enrichment post-library preparation enhances the sensitivity of highthroughput sequencing-based detection and characterization of viruses from complex samples

Enrichment post-library preparation enhances the sensitivity of highthroughput sequencing-based detection and characterization of viruses from complex samples
14    44    1
Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms

Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms
10    37    1
Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index crosstalk and significantly improve sensitivity of massively parallel sequencing

Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index crosstalk and significantly improve sensitivity of massively parallel sequencing
10    54    1
Identification of differentially expressed microRNAs in primary esophageal achalasia by next-generation sequencing

Identification of differentially expressed microRNAs in primary esophageal achalasia by next-generation sequencing
13    63    1
Long-read individual-molecule sequencing reveals CRISPR-induced genetic heterogeneity in human ESCs

Long-read individual-molecule sequencing reveals CRISPR-induced genetic heterogeneity in human ESCs
14    62    1
An amplicon-based sequencing framework for accurately measuring intrahost virus diversity using PrimalSeq and iVar

An amplicon-based sequencing framework for accurately measuring intrahost virus diversity using PrimalSeq and iVar
19    19    1
Opportunities and challenges of whole-genome and exome sequencing

Opportunities and challenges of whole-genome and exome sequencing
13    24    1
Ebook Principles of sequencing and scheduling: Part 1

Ebook Principles of sequencing and scheduling: Part 1
215    11    1
Sequencing of plant genomes - a review

Sequencing of plant genomes - a review
16    76    0
Whole exome sequencing pipeline evaluation and mutation detection in esophageal cancer patients

Whole exome sequencing pipeline evaluation and mutation detection in esophageal cancer patients
9    90    0
Targeted next generation sequencing identifies somatic mutations in a cohort of Egyptian breast cancer patients

Targeted next generation sequencing identifies somatic mutations in a cohort of Egyptian breast cancer patients
9    97    0
A new massively parallel nanoball sequencing platform for whole exome research

A new massively parallel nanoball sequencing platform for whole exome research
9    63    1
Variant detection sensitivity and biases in whole genome and exome sequencing

Variant detection sensitivity and biases in whole genome and exome sequencing
11    52    1