"long read sequencing" trang 2 - tải miễn phí từ tailieunhanh
Meta-aligner: Long-read alignment based on genome statistics

Meta-aligner: Long-read alignment based on genome statistics
9    37    1
Correcting palindromes in long reads after whole-genome amplification

Correcting palindromes in long reads after whole-genome amplification
12    41    1
Genomic repeats, misassembly and reannotation: A case study with long-read resequencing of Porphyromonas gingivalis reference strains

Genomic repeats, misassembly and reannotation: A case study with long-read resequencing of Porphyromonas gingivalis reference strains
24    41    1
Assignment of virus and antimicrobial resistance genes to microbial hosts in a complex microbial community by combined long-read assembly and proximity ligation

Assignment of virus and antimicrobial resistance genes to microbial hosts in a complex microbial community by combined long-read assembly and proximity ligation
18    27    3
Transcriptome assembly from long-read RNA-seq alignments with StringTie2

Transcriptome assembly from long-read RNA-seq alignments with StringTie2
13    40    3
Telomere length de novo assembly of all 7 chromosomes and mitogenome sequencing of the model entomopathogenic fungus, Metarhizium brunneum, by means of a novel assembly pipeline

Telomere length de novo assembly of all 7 chromosomes and mitogenome sequencing of the model entomopathogenic fungus, Metarhizium brunneum, by means of a novel assembly pipeline
15    38    1
Whole genome sequencing of Borrelia miyamotoi isolate Izh-4: Reference for a complex bacterial genome

Whole genome sequencing of Borrelia miyamotoi isolate Izh-4: Reference for a complex bacterial genome
18    46    2
Template-switching artifacts resemble alternative polyadenylation

Template-switching artifacts resemble alternative polyadenylation
10    34    1
Nanopore sequencing reveals endogenous NMD-targeted isoforms in human cells

Nanopore sequencing reveals endogenous NMD-targeted isoforms in human cells
23    63    1
DNA methylation-calling tools for Oxford Nanopore sequencing: A survey and human epigenome-wide evaluation

DNA methylation-calling tools for Oxford Nanopore sequencing: A survey and human epigenome-wide evaluation
33    50    1
Performance of neural network basecalling tools for Oxford Nanopore sequencing

Performance of neural network basecalling tools for Oxford Nanopore sequencing
10    13    1
Long-read cDNA sequencing identifies functional pseudogenes in the human transcriptome

Long-read cDNA sequencing identifies functional pseudogenes in the human transcriptome
15    44    1
Long-read-based human genomic structural variation detection with cuteSV

Long-read-based human genomic structural variation detection with cuteSV
24    48    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
Unveiling the transcriptomic complexity of Miscanthus sinensis using a combination of PacBio long read- and Illumina short read sequencing platforms

Unveiling the transcriptomic complexity of Miscanthus sinensis using a combination of PacBio long read- and Illumina short read sequencing platforms
16    54    1
Linked read technology for assembling large complex and polyploid genomes

Linked read technology for assembling large complex and polyploid genomes
15    24    1
High quality genome assemblies of Mycoplasma bovis using a taxon‑specifc Bonito basecaller for MinION and Flongle long‑read nanopore sequencing

High quality genome assemblies of Mycoplasma bovis using a taxon‑specifc Bonito basecaller for MinION and Flongle long‑read nanopore sequencing
16    52    1
PBHoney: Identifying genomic variants via long-read discordance and interrupted mapping

PBHoney: Identifying genomic variants via long-read discordance and interrupted mapping
7    37    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
A new method for long-read sequencing of animal mitochondrial genomes: Application to the identification of equine mitochondrial DNA variants

A new method for long-read sequencing of animal mitochondrial genomes: Application to the identification of equine mitochondrial DNA variants
15    33    1