Hi,
I have a question about using TopHat. I want to map the reads only using known gene annotations (without discovering any novel splice junctions). Therefore I am using --GTF and --transcriptome-index options. However, I am not sure which option should I use --no-novel-juncs or --transcriptome-only and what is the difference between the two?
For me it seems that whichever options I choose, TopHat still tries to map reads to genome (if they do not map to transcriptome). See below the log file from a run with --transcriptome-only option.
------------
Mon Feb 6 22:18:11 2012] Preparing output location input/GM06985/tophat/
[Mon Feb 6 22:18:11 2012] Checking for Bowtie index files
[Mon Feb 6 22:18:11 2012] Checking for Bowtie index files
[Mon Feb 6 22:18:11 2012] Checking for reference FASTA file
[Mon Feb 6 22:18:11 2012] Checking for Bowtie
Bowtie version: 0.12.7.0
[Mon Feb 6 22:18:11 2012] Checking for Samtools
Samtools Version: 0.1.16
[Mon Feb 6 22:18:11 2012] Generating SAM header for hg19
format: fastq
quality scale: phred33 (default)
[Mon Feb 6 22:18:35 2012] Reading known junctions from GTF file
[Mon Feb 6 22:18:52 2012] Preparing reads
left reads: min. length=50, count=38337749
[Mon Feb 6 22:29:55 2012] Using pre-built transcriptome index..
[Mon Feb 6 22:29:55 2012] Mapping left_kept_reads against transcriptome known with Bowtie
[Mon Feb 6 23:19:26 2012] Converting left_kept_reads.m2g to genomic coordinates (map2gtf)
[Mon Feb 6 23:54:00 2012] Resuming TopHat pipeline with unmapped reads
[Mon Feb 6 23:54:00 2012] Mapping left_kept_reads.m2g_um against hg19 with Bowtie
[Tue Feb 7 01:08:53 2012] Processing bowtie hits
[Tue Feb 7 01:25:39 2012] Mapping left_kept_reads.m2g_um_seg1 against hg19 with Bowtie (1/2)
[Tue Feb 7 02:20:36 2012] Mapping left_kept_reads.m2g_um_seg2 against hg19 with Bowtie (2/2)
[Tue Feb 7 03:06:23 2012] Searching for junctions via segment mapping
[Tue Feb 7 04:43:56 2012] Retrieving sequences for splices
[Tue Feb 7 05:08:27 2012] Indexing splices
[Tue Feb 7 05:19:54 2012] Mapping left_kept_reads.m2g_um_seg1 against segment_juncs with Bowtie (1/2)
[Tue Feb 7 05:49:43 2012] Mapping left_kept_reads.m2g_um_seg2 against segment_juncs with Bowtie (2/2)
[Tue Feb 7 06:17:11 2012] Joining segment hits
[Tue Feb 7 06:36:14 2012] Reporting output tracks
Unconfigured Ad
Collapse
Latest Articles
Collapse
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
-
by SEQadmin2
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
Channel: Articles
-
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 10-22-2026, 11:13 AM
|
0 responses
27 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 11:13 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 10:48 AM
|
0 responses
20 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 10:48 AM
|
||
|
Started by SEQadmin2, 10-15-2026, 10:52 AM
|
0 responses
36 views
0 reactions
|
Last Post
by SEQadmin2
10-15-2026, 10:52 AM
|
||
|
Started by SEQadmin2, 10-14-2026, 05:39 AM
|
0 responses
43 views
0 reactions
|
Last Post
by SEQadmin2
10-14-2026, 05:39 AM
|