Unlock your biological data

?

Alignment evaluation software tools | High-throughput sequencing data analysis

Alignment evaluation software tools | High-throughput sequencing data analysis

Accurate mapping of next-generation sequencing (NGS) reads to reference genomes is crucial for almost all NGS applications and downstream analyses. Various repetitive elements in human and other higher eukaryotic genomes contribute in large part to ambiguously (non-uniquely) mapped reads. Most available NGS aligners attempt to address this by either removing all non-uniquely mapping reads, or reporting one random or "best" hit based on simple heuristics. Accurate estimation of the mapping quality of NGS reads is therefore critical albeit completely lacking at present.

1 - 20 of 34 results
filter_list Filters
build Technology
laptop Operating System
desktop_windows Interface
important_devices Computer Skill
copyright Restriction to use
memory Programming Language
import_contacts Journal
account_balance Funding
1 - 20 of 34 results
0 - 0 of 0 results
1 - 20 of 25 results
filter_list Filters
business_center Job seeker
Disable 8
assignment_ind Position
public Country
memory Programming Language
1 - 20 of 40 results
filter_list Filters
apps Application
settings Tool
build Technology
laptop Operating System
desktop_windows Interface
important_devices Computer Skill
copyright Restriction to use
memory Programming Language
healing Disease
pets Taxonomy
grain Chemical
import_contacts Journal
1 - 20 of 40 results