Header Leaderboard Ad

Collapse

On/off target rate for whole exome data

Collapse

Announcement

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

  • On/off target rate for whole exome data

    Hi all,

    I've some human exome data, which I've aligned with bowtie2 as bwa doesn't work (see this post).

    Using samtools flagstat I can see ~98% of reads map to the genome. However, only about 60% of those are on-target with 40% off-target. That doesn't seem great.

    What kind of on/off-target rates do others see?

  • #2
    Originally posted by chris View Post
    Hi all,

    I've some human exome data, which I've aligned with bowtie2 as bwa doesn't work (see this post).

    Using samtools flagstat I can see ~98% of reads map to the genome. However, only about 60% of those are on-target with 40% off-target. That doesn't seem great.

    What kind of on/off-target rates do others see?
    Actually, that's about what the people selling the kits promise, so you are fine.

    Comment


    • #3
      Originally posted by chris View Post
      Hi all,

      I've some human exome data, which I've aligned with bowtie2 as bwa doesn't work (see this post).

      Using samtools flagstat I can see ~98% of reads map to the genome. However, only about 60% of those are on-target with 40% off-target. That doesn't seem great.

      What kind of on/off-target rates do others see?
      Don't worry - perfectly acceptable figures there.

      Comment


      • #4
        Great. Thanks.

        Comment


        • #5
          @chris -- would you care to share your command line for bowtie2? I'm running into a slightly worse issue, performance wise, and am curious how you're doing it!

          Comment


          • #6
            Sure, its:

            Code:
            bowtie2 --threads 4 -q --sensitive --end-to-end --phred33 -x /db/bowtie2/Hsapiens68 -1 fastq_file1 -2 fastq_file1 -S out.sam

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Improved Targeted Sequencing: A Comprehensive Guide to Amplicon Sequencing
              by seqadmin



              Amplicon sequencing is a targeted approach that allows researchers to investigate specific regions of the genome. This technique is routinely used in applications such as variant identification, clinical research, and infectious disease surveillance. The amplicon sequencing process begins by designing primers that flank the regions of interest. The DNA sequences are then amplified through PCR (typically multiplex PCR) to produce amplicons complementary to the targets. RNA targets...
              03-21-2023, 01:49 PM
            • seqadmin
              Targeted Sequencing: Choosing Between Hybridization Capture and Amplicon Sequencing
              by seqadmin




              Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...
              03-10-2023, 05:31 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 03-24-2023, 02:45 PM
            0 responses
            16 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-22-2023, 12:26 PM
            0 responses
            17 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-17-2023, 12:32 PM
            0 responses
            17 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 03-15-2023, 12:42 PM
            0 responses
            24 views
            0 likes
            Last Post seqadmin  
            Working...
            X