Hello Hong-Bi,
Thank you for your interest in the Genome Browser.
We were not able to identify what file the information you provided came from. The file lists unique gene symbols with a single exon start/end coordinate for each entry, but does not exactly match any schemas we provide. It seems there were some post-download modifications.
If you are looking for unique gene data on the hg38 assembly, however, we can help you get that. Using the Table Browser (http://genome.ucsc.edu/cgi-bin/hgTables), you can make the following selections to get one transcript per gene symbol for the whole genome:
Your output file should look as such:
It includes the chromosome, the transcription start (beginning of first exon), transcription end (end of final exon), and gene symbol. You may also wish to include strand information to include all the data in the files you provided.
I hope this is helpful. If you have any further questions, please reply to gen...@soe.ucsc.edu. All messages sent to that address are archived on a publicly-accessible Google Groups forum. If your question includes sensitive data, you may send it instead to genom...@soe.ucsc.edu.
Lou Nassar
UCSC Genomics Institute
Training videos & resources: http://genome.ucsc.edu/training/index.html
Want to share the Browser with colleagues?
Host a workshop: http://bit.ly/ucscTraining
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And the data that i exactly want is gene Transcript position including UTRs.I think I should change following selections, don't I?please let me know, thank you.Your sincerelyHong-Bi Kim2019년 9월 2일 (월) 오후 5:45, 김홍비[학생](약학대학 한약학과) <tir4r...@khu.ac.kr>님이 작성:Thank you for your reply.But I had a problem in searching data.You said i should select track as USCS Genes. But I couldn't find USCS Genes. As you can see picture below, there is no USCS Genes. In this situation, how can i do?
- track: UCSC Genes
Your sincerelyHong-Bi Kim2019년 8월 28일 (수) 오전 12:39, Luis Nassar <lrna...@ucsc.edu>님이 작성:
--Hong Bi KimUndergraduate StudentDepartment of Life and Nanopharmaceutical ScienceB210 College of Pharmacy, Kyung Hee University26 Kyunghee-daero, Dongdaemoon-guSeoul 02447Republic of KoreaCELL: +82-10-3202-5050 / EMAIL : tir4r...@khu.ac.kr--Hong Bi KimUndergraduate StudentDepartment of Life and Nanopharmaceutical ScienceB210 College of Pharmacy, Kyung Hee University26 Kyunghee-daero, Dongdaemoon-guSeoul 02447Republic of KoreaCELL: +82-10-3202-5050 / EMAIL : tir4r...@khu.ac.kr
Hello Hong-Bi,
I apologize for mentioning the UCSC Genes track. That is the track that corresponds to these steps for the hg19 assembly. For the hg38 assembly, you will want to select GENCODE v29.
The steps would be the same as my previous response except for the track name. These steps will generate one transcript per gene symbol for the whole genome. These coordinates are transcription start/end, so they include UTRs:
If you would instead like to get all transcripts, and not just one representation per gene, you can make the following selections. These will also give you transcription start/end, along with ENSEMBL id and associated gene symbol:
Those results should look as follows:
If you have any further questions, please reply to gen...@soe.ucsc.edu. All messages sent to that address are archived on a publicly-accessible Google Groups forum. If your question includes sensitive data, you may send it instead to genom...@soe.ucsc.edu.
Lou Nassar
UCSC Genomics Institute
Training videos & resources: http://genome.ucsc.edu/training/index.html
Want to share the Browser with colleagues?
Host a workshop: http://bit.ly/ucscTraining
| chromStart | Start position (0 based). Represents transcription start for + strand genes, end for - strand genes | |
| chromEnd | End position (non-inclusive). Represents transcription end for + strand genes, start for - strand genes |
| hg38 | knownGene | Transcript from default gene set in UCSC browser |
| strand | + or - for strand |
Thank you for your helping.I can get gene location file following your mails.I also need direction in which genes are coded, but the file that you inform me only includes the location of gene.Let me explain what I want.For example, DNA is double strand.So, exonstart of PRR26 is 649947 and exonend of PRR26 is 665169. Its direction is small number to big number. I will call it (+) strand.exonstart of TUBB8 is 49504 and exonend of TUBB8 is 46436. Its direction is big number to small number. I will call it (-) strand.But in the file that you inform me, all of end is bigger than all of start. I think it didn't considered direction.
please let me know, thank you.Your sincerelyHong-Bi Kim
2019년 9월 4일 (수) 오전 6:26, Luis Nassar <lrna...@ucsc.edu>님이 작성: