![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Uploading BAM Track to UCSC Genome Browser | jjw14 | Bioinformatics | 4 | 02-01-2019 08:15 AM |
Bedgraph file upload in UCSC browser - error | anagari | Bioinformatics | 6 | 11-20-2012 09:56 PM |
not able to load a bed file into UCSC genome browser | ataaillah | Introductions | 0 | 01-18-2012 08:46 AM |
Upload .bam file to Galaxy, display on UCSC | biznatch | Bioinformatics | 3 | 12-20-2011 04:12 PM |
BAM file to Histogram on UCSC Genome Browser | qnc | Bioinformatics | 3 | 10-14-2011 07:11 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Junior Member
Location: Brazil Join Date: Dec 2010
Posts: 3
|
![]()
I 'm a newbie in mapping stuff, so I'm training mapping 454 reads, first of all I mapped one file that I got in sra database... so I mapped it using bwa, genereted an sam file... I converted to bam....
but when I try to upload to http://genome.ucsc.edu/cgi-bin/hgCustom , using the browser to upload directly from my PC and click "submit", it says that Can't read file.bam !!! Can someone help me ?? I know that there is other way to upload , hosting the file into a link... but I don 't have where to host my file.bam ![]() |
![]() |
![]() |
![]() |
#2 |
Senior Member
Location: 45°30'25.22"N / 9°15'53.00"E Join Date: Apr 2009
Posts: 258
|
![]()
You don't have to upload a bam file. You need to have it visible at a certain ftp or http uri, then add
track type=bam bigDataUrl=http://link/to/your/bam/file just be sure you have indexed the bam file. d |
![]() |
![]() |
![]() |
#3 |
Senior Member
Location: Graz, Austria Join Date: Feb 2010
Posts: 219
|
![]()
Just in case your BAM file is too large, you could split it and index the splitted parts.
In case your BAM File is broken: you could check that out using the picard validateSamFile option. But in any case: uploading a large BAM file is slow and loading the data over an external http/ftp server certainly would be a good idea. If you only plan to visualize your alignments you could use stanalone visualization prgrams like IGV, Savant or different others. They also can visualize accompanying data if you got them in the right data format. That would save you some time and issues of uploading... |
![]() |
![]() |
![]() |
#4 |
Member
Location: Bethesda, MD Join Date: Apr 2009
Posts: 51
|
![]()
I will second the use of IGV from Broad. It's a great tool to locally view alignments.
http://www.broadinstitute.org/igv/ |
![]() |
![]() |
![]() |
#5 |
Junior Member
Location: Brazil Join Date: Dec 2010
Posts: 3
|
![]()
sorry for the late answer!
thanks all for your help... I used picard to validatesam to my bam file and thats what happened ERROR: Read groups is empty WARNING: Record 1, Read name SRR013983.23952, NM tag (nucleotide differences) is missing WARNING: Record 2, Read name SRR013983.59880, NM tag (nucleotide differences) is missing WARNING: Record 3, Read name SRR013983.22265, NM tag (nucleotide differences) is missing and etc..... do u know what is happening? thnks |
![]() |
![]() |
![]() |
Thread Tools | |
|
|