| Literature DB >> 24685334 |
Jesus Enrique Herrera-Galeano1, Kenneth G Frey, Regina Z Cer, Alfred J Mateczun, Kimberly A Bishop-Lilly, Vishwesh P Mokashi.
Abstract
BACKGROUND: The development of Next Generation Sequencing (NGS) during the last decade has created an unprecedented amount of sequencing data, as well as the ability to rapidly sequence specimens of interest. Read-based BLAST analysis of NGS data is a common procedure especially in the case of metagenomic samples. However, coverage is usually not enough to allow for de novo assembly. This type of read-based analysis often creates the question of how the reads that align to the same sequence are distributed. The same question applies to preparation of primers or probes for microarray experiments. Although there are several packages that allow the visualization of DNA segments in relation to a reference, in most cases they require the visualization of one reference at a time and the capture of screen shots for each segment. Such a procedure could be tedious and time consuming. The field is in need of a solution that automates the capture of coverage plots for all the segments of interest.Entities:
Year: 2014 PMID: 24685334 PMCID: PMC3974413 DOI: 10.1186/1751-0473-9-7
Source DB: PubMed Journal: Source Code Biol Med ISSN: 1751-0473
Figure 1Shows the distribution of primers for HIV-1 sequence. A. CD.02._02CD_KTB035.AM000055, upper left corner, is the sequence identifier. 1, on the other middle left, is the start of sequence. 9740 on the middle right is the end of the sequence. (A) shows the position on the reference where the match with the query starts. (B) shows the position on the reference where the match with the query ends. (C) shows the count of primers that map to the same location (if it is greater the one). (D) shows the identifier for the query.