Results 21 to 30 of about 9,152,640 (254)

Long-read whole genome sequencing of human T cells

open access: yes, 2023
This dataset represent long read sequencing of single human T cells isolated from a human donor. The data set include Illumina whole genome sequencing of 16 single T cells and PacBio HiFi whole genome sequenicng of 5 single T cells   
Joanna Hård (10518953)   +1 more
core   +2 more sources

long-read-tools.org: an interactive catalogue of analysis methods for long-read sequencing data

open access: yes, 2021
© The Author(s) 2021. Published by Oxford University Press GigaScience. BACKGROUND: The data produced by long-read third-generation sequencers have unique characteristics compared to short-read sequencing data, often requiring tailored analysis tools for
ME Ritchie (9757601)   +2 more
core   +1 more source

Summary of the long-read sequencing data.

open access: yes, 2023
(A) The sequencing depth (left) and reads N50 (right) of long-read data obtained from 21 pairs of tumor/ normal samples via nanopore sequencer. (B) Cumulative distribution of total bases (Y axis) over read length (X axis) for tumor/ normal samples.
Xiaohuan Lu (5583656)   +9 more
core   +1 more source

Long-read sequencing report with Oxford Nanopore Technologies of different soil samples using different DNA extraction methods.

open access: yes, 2023
Long-read sequencing report with Oxford Nanopore Technologies of different soil samples using different DNA extraction ...
Andrey Zamyatnin (16857811)   +4 more
core   +1 more source

HAT: de novo variant calling for highly accurate short-read and long-read sequencing data [PDF]

open access: yes, 2023
MOTIVATION: de novo variant (DNV) calling is challenging from parent-child sequenced trio data. We developed H are A nd T ortoise (HAT) to work as an automated workflow to detect DNVs in highly accurate short-read and long-read sequencing data.
Ng, Jeffrey K.   +5 more
core   +1 more source

Long-read sequencing report with Oxford Nanopore Technologies of different soil samples using different DNA extraction methods (Report 20.02.2023)

open access: yes, 2023
Long-read sequencing report with Oxford Nanopore Technologies of different soil samples using different DNA extraction methods.
Andrey Zamyatnin (16857811)   +4 more
core   +1 more source

Long-Read Sequencing Annotation of the Transcriptome in DNA-PK Inactivated Cells

open access: yesFrontiers in Oncology, 2022
The DNA-dependent protein kinase catalytic subunit (DNA-PKcs) with a Ku70/Ku80 heterodimer constitutes the intact DNA-PK kinase, which is an upstream component of the DNA repair machinery that signals the DNA damage, orchestrates the DNA repair, and ...
Liwei Song   +10 more
doaj   +1 more source

Sequencing output of short- and long-read RNA-seq.

open access: yes, 2023
Sequencing output of short- and long-read RNA-seq.
Johnathon M. Hall (8431497)   +3 more
core   +1 more source

Long-Read Sequencing Emerging in Medical Genetics

open access: yesFrontiers in Genetics, 2019
The wide implementation of next-generation sequencing (NGS) technologies has revolutionized the field of medical genetics. However, the short read lengths of currently used sequencing approaches pose a limitation for the identification of structural ...
Tuomo Mantere   +7 more
doaj   +1 more source

QitanTech Nanopore Long-Read Sequencing Enables Rapid Resolution of Complete Genomes of Multi-Drug Resistant Pathogens

open access: yesFrontiers in Microbiology, 2022
Advancement of novel sequencing technologies facilitates modern life science and medicine unprecedentedly. Exploring complete genome sequences of bacteria by long-read sequencing technology is significant for microbial genomics research.
Kai Peng   +13 more
doaj   +1 more source

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