Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Brian Bushnell
    replied
    Adrian,

    You can try running repair.sh to split the file into paired and unpaired reads, and then map twice, once for the paired and once for the unpaired, and then merge the bam files. That will allow maximal use of the available information.

    Leave a comment:


  • adrian
    replied
    Yes thats a disadvantage I agree.

    Unfortunately, the bam file does not have enough PE reads.

    When I used bamtofastq for PE fastq files, interestingly I obtained 0 fastq reads.

    Leave a comment:


  • dpryan
    replied
    Yes, you'll be expected to decrease your mapping efficiency a bit, since one mate can act as an anchor to rescue the other. Further, it's much easier to use paired-end reads to find isoforms, since you're then not relying solely on alignments over a splice junction.

    Leave a comment:


  • converting paired-end (PE) bam file to single-end (SE) fastq

    Hi:
    while working with COAD TCGA BAM files, I find the very annoying to find PE reads. These files are mashed up and not consistent.
    for example:
    1. read lengths are not consistent. Some are 34 some 76 reads.
    2. Many reads miss mate or pair.

    I want to identify novel splicing differences however TCGA BAM files are mapped to known transcripts (known exon pairing from known isoforms gtf) thus limiting the discovery of novel isoforms.

    I decided convert BAM to fastq and realign to full genome.

    While doing this, because of loss of many pair and mates in bam, I converted them to single end fastq.

    Any ideas if converting a paired-end bam to single end fastq pose any problem in philosophical ways.

    thanks

Latest Articles

Collapse

  • seqadmin
    Advancing Precision Medicine for Rare Diseases in Children
    by seqadmin




    Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
    12-16-2024, 07:57 AM
  • seqadmin
    Recent Advances in Sequencing Technologies
    by seqadmin



    Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

    Long-Read Sequencing
    Long-read sequencing has seen remarkable advancements,...
    12-02-2024, 01:49 PM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by seqadmin, 12-17-2024, 10:28 AM
0 responses
26 views
0 likes
Last Post seqadmin  
Started by seqadmin, 12-13-2024, 08:24 AM
0 responses
42 views
0 likes
Last Post seqadmin  
Started by seqadmin, 12-12-2024, 07:41 AM
0 responses
28 views
0 likes
Last Post seqadmin  
Started by seqadmin, 12-11-2024, 07:45 AM
0 responses
42 views
0 likes
Last Post seqadmin  
Working...
X