Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • ibf123
    Junior Member
    • Dec 2018
    • 1

    Alignment verification IGV

    Hello folks,

    Fairly new to RNA-Seq so here are some quality control questions I've come across and cannot seem to find a good answer to.

    After I quality control check my samples with FastQC and proceed with Hisat and samtools, I then check the alignments made using IGV.

    However, I've noticed that some of the genes are out by roughly 10-30bp from the reference genome (human 38). Is that ok?

    Secondly, if reads map to very few bps for a gene is that gene still a credible hit?

    And lastly, is there any concern about having identical mappings of individual genes between different samples?

    Thank you.
  • ashishbansal
    Member
    • Dec 2018
    • 17

    #2
    To view aligned reads using the*Integrative Genomics Viewer (IGV), the SAM or BAM file must be coordinate-sorted and indexed.
    1. Always load the reference genome first. Go to*Genomes>Load Genome From Server*or load from the drop-down menu in the upper left corner. Select*Human (1kg, b37+decoy).
    2. Load the data file. Go to*File>Load from File*and select*6491_snippet.bam. IGV automatically uses the corresponding*6491_snippet.bai*index in the same folder.
    3. Zoom in to see alignments. For our tutorial data, copy and paste*10:96,867,400-96,869,400*into the textbox at the top and press*Go. A 2 kbp region of chromosome 10 comes into view as shown in the screenshot above.
    Alongside read data, IGV automatically generates a coverage track that sums the depth of reads for each genomic position.
    4. Right-click on the alignment track and*Select by name. Copy and paste*H0164ALXX140820:2:2107:7323:30703*into the read name textbox and press*OK. IGV will highlight two reads corresponding to this query name in bold red.
    5. Right-click on the alignment track and select*View as pairs. The two highlighted reads will display in the same row connected by a line as shown in the screenshot.
    Because IGV holds in memory a limited set of data overlapping with the genomic interval in view (this is what makes IGV fast), the*select by name*feature also applies only to the data that you call into view. For example, we know this read has a secondary alignment on contig hs37d5 (hs37d5:10,198,000-10,200,000).
    Clinical Research

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Nine Things a Sample Prep Scientist Thinks About Before Sequencing
      by SEQadmin2


      I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.


      Here are nine questions we think about, in roughly the order they matter, before...
      06-18-2026, 07:11 AM
    • SEQadmin2
      From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
      by SEQadmin2


      Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


      The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
      ...
      06-02-2026, 10:05 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 06-17-2026, 06:09 AM
    0 responses
    30 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-09-2026, 11:58 AM
    0 responses
    96 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-05-2026, 10:09 AM
    0 responses
    116 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-04-2026, 08:59 AM
    0 responses
    109 views
    0 reactions
    Last Post SEQadmin2  
    Working...