"Read alignment" trang 1 - tải miễn phí từ tailieunhanh
A sensitive short read homology search tool for paired-end read sequencing data

A sensitive short read homology search tool for paired-end read sequencing data
13    57    1
Towards pan-genome read alignment to improve variation calling

Towards pan-genome read alignment to improve variation calling
8    60    1
Probabilistic alignment leads to improved accuracy and read coverage for bisulfite sequencing data

Probabilistic alignment leads to improved accuracy and read coverage for bisulfite sequencing data
8    39    1
Oculus: Faster sequence alignment by streaming read compression

Oculus: Faster sequence alignment by streaming read compression
8    40    1
Cloud accelerated alignment and assembly of full-length single-cell RNA-seq data using Falco

Cloud accelerated alignment and assembly of full-length single-cell RNA-seq data using Falco
12    37    2
Alignment and mapping methodology influence transcript abundance estimation

Alignment and mapping methodology influence transcript abundance estimation
29    49    1
Meta-aligner: Long-read alignment based on genome statistics

Meta-aligner: Long-read alignment based on genome statistics
9    37    1
LSCplus: A fast solution for improving long read accuracy by short read alignment

LSCplus: A fast solution for improving long read accuracy by short read alignment
9    50    1
Improving read mapping using additional prefix grams

Improving read mapping using additional prefix grams
11    31    1
Novel read density distribution score shows possible aligner artefacts, when mapping a single chromosome

Novel read density distribution score shows possible aligner artefacts, when mapping a single chromosome
11    37    1
BWTaligner: a genome short-read aligner

BWTaligner: a genome short-read aligner
5    55    0
Assessing graph-based read mappers against a baseline approach highlights strengths and weaknesses of current methods

Assessing graph-based read mappers against a baseline approach highlights strengths and weaknesses of current methods
9    34    2
Báo cáo y học:

Báo cáo y học: "Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA"
12    35    0
A short note on dynamic programming in a band

A short note on dynamic programming in a band
5    39    1
Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection

Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection
16    47    1
Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles

Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles
8    45    1
Adaptable probabilistic mapping of short reads using position specific scoring matrices

Adaptable probabilistic mapping of short reads using position specific scoring matrices
17    62    1
Blind spots of quantitative RNA-seq: The limits for assessing abundance, differential expression, and isoform switching

Blind spots of quantitative RNA-seq: The limits for assessing abundance, differential expression, and isoform switching
10    32    1
Diminishing return for increased Mappability with longer sequencing reads: Implications of the k-mer distributions in the human genome

Diminishing return for increased Mappability with longer sequencing reads: Implications of the k-mer distributions in the human genome
12    52    1
Benchmarking variant identification tools for plant diversity discovery

Benchmarking variant identification tools for plant diversity discovery
15    34    1