how to transfer gene id into protein id
Hi, I have some refseq gene id, like NM_*****. How can I transfer these gene id into protein id, like NP_****? Thank you very much! Victor
Hello, If the reference genome is in UCSC and has a RefSeq track, then you can extract a file with the transcript and protein identifiers from the Table Browser called "refLink" and subset it for rows in your query RefSeq transcript identifiers. If the RefSeq data is at BioMart or another source, a similar path to the one I outline below will work with some modifications, it all depends on the file format, but Galaxy's tools can manipulate data is just about every way you will need. Using a transcript identifier query, subset protein identifiers in a UCSC RefSeq track: A. Load your list of NM* identifiers ("Get Data -> Upload). - set the file format to "tabular" (use "pencil" icon to "Edit Attributes -> Change data type") if needed. B. Load RefSeq id mapping data with "Get Data -> UCSC Main" and set the form parameters as needed, choosing the track "RefSeq Genes" and the table "refLink". Make sure the region is the entire genome. Send to Galaxy formatted as-is (tabular). B. Next, cut columns 3 and 4 out of the table with tool "Text Manipulation ->Cut" and the options "c3,c4". C. OPTIONAL, if you want the full list of coding RefSeqs for another purpose... remove the non-coding RefSeqs with the tool "Filter and Sort -> Select" and the options "that: NOT Matching" and "the pattern: ^NR_.*$". Be sure to enter the regular expression '^NR_.*$' without any quotes. D. Perform a join using "Join, Subtract and Group -> Compare two Datasets" with the options>: - "Compare: <file of trans and prot id, filtered or not>" - "Using column: c1" where c1 is the trans ids - "against: <file of trans ids>" - "and column: c1" where c1 is the trans ids - "To find: Matching rows of first dataset" E. Result dataset is a two column tabular file: transcript id <tab> protein id Hopefully this helps you and others who are doing a similar task. If you think you will be doing this a lot, be sure to consider extracting the steps into a workflow. Thanks for using Galaxy, Jen Galaxy team On 10/27/11 1:34 PM, Li, Jilong (MU-Student) wrote:
Hi,
I have some refseq gene id, like NM_*****.
How can I transfer these gene id into protein id, like NP_****?
Thank you very much!
Victor
___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
-- Jennifer Jackson http://usegalaxy.org http://galaxyproject.org/wiki/Support
Hi, I have some refseq gene id, like NM_***** and NR_******. I know how to transfer NM_****** into protein ID NP_*****. But, how to transfer NR_***** into protein id, like NP_****? I do not know. Could you please tell me? Thank you very much! Victor ________________________________________ From: Jennifer Jackson [jen@bx.psu.edu] Sent: Thursday, October 27, 2011 11:23 PM To: Li, Jilong (MU-Student) Cc: galaxy-user@bx.psu.edu Subject: Re: [galaxy-user] how to transfer gene id into protein id Hello, If the reference genome is in UCSC and has a RefSeq track, then you can extract a file with the transcript and protein identifiers from the Table Browser called "refLink" and subset it for rows in your query RefSeq transcript identifiers. If the RefSeq data is at BioMart or another source, a similar path to the one I outline below will work with some modifications, it all depends on the file format, but Galaxy's tools can manipulate data is just about every way you will need. Using a transcript identifier query, subset protein identifiers in a UCSC RefSeq track: A. Load your list of NM* identifiers ("Get Data -> Upload). - set the file format to "tabular" (use "pencil" icon to "Edit Attributes -> Change data type") if needed. B. Load RefSeq id mapping data with "Get Data -> UCSC Main" and set the form parameters as needed, choosing the track "RefSeq Genes" and the table "refLink". Make sure the region is the entire genome. Send to Galaxy formatted as-is (tabular). B. Next, cut columns 3 and 4 out of the table with tool "Text Manipulation ->Cut" and the options "c3,c4". C. OPTIONAL, if you want the full list of coding RefSeqs for another purpose... remove the non-coding RefSeqs with the tool "Filter and Sort -> Select" and the options "that: NOT Matching" and "the pattern: ^NR_.*$". Be sure to enter the regular expression '^NR_.*$' without any quotes. D. Perform a join using "Join, Subtract and Group -> Compare two Datasets" with the options>: - "Compare: <file of trans and prot id, filtered or not>" - "Using column: c1" where c1 is the trans ids - "against: <file of trans ids>" - "and column: c1" where c1 is the trans ids - "To find: Matching rows of first dataset" E. Result dataset is a two column tabular file: transcript id <tab> protein id Hopefully this helps you and others who are doing a similar task. If you think you will be doing this a lot, be sure to consider extracting the steps into a workflow. Thanks for using Galaxy, Jen Galaxy team On 10/27/11 1:34 PM, Li, Jilong (MU-Student) wrote:
Hi,
I have some refseq gene id, like NM_*****.
How can I transfer these gene id into protein id, like NP_****?
Thank you very much!
Victor
___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
-- Jennifer Jackson http://usegalaxy.org http://galaxyproject.org/wiki/Support
Hello Victor, RefSeq sequences designated by a transcript identifier formatted as NR_* are non-coding (meaning: transcribed, but not translated), therefore there is no protein product and no linked protein sequence NP_* identifier. This documentation from NCBI covers RefSeq naming conventions: http://www.ncbi.nlm.nih.gov/RefSeq/key.html Hopefully this is helpful, Best, Jen Galaxy team On 10/28/11 3:24 PM, Li, Jilong (MU-Student) wrote:
Hi,
I have some refseq gene id, like NM_***** and NR_******.
I know how to transfer NM_****** into protein ID NP_*****. But, how to transfer NR_***** into protein id, like NP_****? I do not know. Could you please tell me?
Thank you very much!
Victor
________________________________________ From: Jennifer Jackson [jen@bx.psu.edu] Sent: Thursday, October 27, 2011 11:23 PM To: Li, Jilong (MU-Student) Cc: galaxy-user@bx.psu.edu Subject: Re: [galaxy-user] how to transfer gene id into protein id
Hello,
If the reference genome is in UCSC and has a RefSeq track, then you can extract a file with the transcript and protein identifiers from the Table Browser called "refLink" and subset it for rows in your query RefSeq transcript identifiers.
If the RefSeq data is at BioMart or another source, a similar path to the one I outline below will work with some modifications, it all depends on the file format, but Galaxy's tools can manipulate data is just about every way you will need.
Using a transcript identifier query, subset protein identifiers in a UCSC RefSeq track:
A. Load your list of NM* identifiers ("Get Data -> Upload). - set the file format to "tabular" (use "pencil" icon to "Edit Attributes -> Change data type") if needed.
B. Load RefSeq id mapping data with "Get Data -> UCSC Main" and set the form parameters as needed, choosing the track "RefSeq Genes" and the table "refLink". Make sure the region is the entire genome. Send to Galaxy formatted as-is (tabular).
B. Next, cut columns 3 and 4 out of the table with tool "Text Manipulation ->Cut" and the options "c3,c4".
C. OPTIONAL, if you want the full list of coding RefSeqs for another purpose... remove the non-coding RefSeqs with the tool "Filter and Sort -> Select" and the options "that: NOT Matching" and "the pattern: ^NR_.*$". Be sure to enter the regular expression '^NR_.*$' without any quotes.
D. Perform a join using "Join, Subtract and Group -> Compare two Datasets" with the options>: - "Compare:<file of trans and prot id, filtered or not>" - "Using column: c1" where c1 is the trans ids - "against:<file of trans ids>" - "and column: c1" where c1 is the trans ids - "To find: Matching rows of first dataset"
E. Result dataset is a two column tabular file: transcript id<tab> protein id
Hopefully this helps you and others who are doing a similar task. If you think you will be doing this a lot, be sure to consider extracting the steps into a workflow.
Thanks for using Galaxy,
Jen Galaxy team
On 10/27/11 1:34 PM, Li, Jilong (MU-Student) wrote:
Hi,
I have some refseq gene id, like NM_*****.
How can I transfer these gene id into protein id, like NP_****?
Thank you very much!
Victor
___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
-- Jennifer Jackson http://usegalaxy.org http://galaxyproject.org/wiki/Support
___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
-- Jennifer Jackson http://usegalaxy.org http://galaxyproject.org/wiki/Support
Hi Victor It is not really a Galaxy related answer....but you might wanna study the following webpage explaining the RefSeq Accession Format: http://www.ncbi.nlm.nih.gov/RefSeq/key.html#accession Strictly speaking, there is no such thing as a "refseq gene id", since RefSeq entries describe individual molecules. There is a new subset of RefSeq called 'RefSeqGene", see: http://www.ncbi.nlm.nih.gov/refseq/rsg/ but I don't think this is what you are after. Hence, you can crosslink 'mRNA' (ie: NM_*****) to proteins (ie: NP_*****) and Jen gave you an excellent recipe how to do that in Galaxy. However, you cannot crosslink 'RNA' (ie: NR_*****, which are "non-coding transcripts including structural RNAs, transcribed pseudogenes, and others.") to proteins! I hope this clarifies the confusion. Regards, Hans On 10/29/2011 12:24 AM, Li, Jilong (MU-Student) wrote:
Hi,
I have some refseq gene id, like NM_***** and NR_******.
I know how to transfer NM_****** into protein ID NP_*****. But, how to transfer NR_***** into protein id, like NP_****? I do not know. Could you please tell me?
Thank you very much!
Victor
________________________________________ From: Jennifer Jackson [jen@bx.psu.edu] Sent: Thursday, October 27, 2011 11:23 PM To: Li, Jilong (MU-Student) Cc: galaxy-user@bx.psu.edu Subject: Re: [galaxy-user] how to transfer gene id into protein id
Hello,
If the reference genome is in UCSC and has a RefSeq track, then you can extract a file with the transcript and protein identifiers from the Table Browser called "refLink" and subset it for rows in your query RefSeq transcript identifiers.
If the RefSeq data is at BioMart or another source, a similar path to the one I outline below will work with some modifications, it all depends on the file format, but Galaxy's tools can manipulate data is just about every way you will need.
Using a transcript identifier query, subset protein identifiers in a UCSC RefSeq track:
A. Load your list of NM* identifiers ("Get Data -> Upload). - set the file format to "tabular" (use "pencil" icon to "Edit Attributes -> Change data type") if needed.
B. Load RefSeq id mapping data with "Get Data -> UCSC Main" and set the form parameters as needed, choosing the track "RefSeq Genes" and the table "refLink". Make sure the region is the entire genome. Send to Galaxy formatted as-is (tabular).
B. Next, cut columns 3 and 4 out of the table with tool "Text Manipulation ->Cut" and the options "c3,c4".
C. OPTIONAL, if you want the full list of coding RefSeqs for another purpose... remove the non-coding RefSeqs with the tool "Filter and Sort -> Select" and the options "that: NOT Matching" and "the pattern: ^NR_.*$". Be sure to enter the regular expression '^NR_.*$' without any quotes.
D. Perform a join using "Join, Subtract and Group -> Compare two Datasets" with the options>: - "Compare:<file of trans and prot id, filtered or not>" - "Using column: c1" where c1 is the trans ids - "against:<file of trans ids>" - "and column: c1" where c1 is the trans ids - "To find: Matching rows of first dataset"
E. Result dataset is a two column tabular file: transcript id<tab> protein id
Hopefully this helps you and others who are doing a similar task. If you think you will be doing this a lot, be sure to consider extracting the steps into a workflow.
Thanks for using Galaxy,
Jen Galaxy team
On 10/27/11 1:34 PM, Li, Jilong (MU-Student) wrote:
Hi,
I have some refseq gene id, like NM_*****.
How can I transfer these gene id into protein id, like NP_****?
Thank you very much!
Victor
___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
-- Jennifer Jackson http://usegalaxy.org http://galaxyproject.org/wiki/Support
___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list:
http://lists.bx.psu.edu/listinfo/galaxy-dev
To manage your subscriptions to this and other Galaxy lists, please use the interface at:
participants (3)
-
Hans-Rudolf Hotz -
Jennifer Jackson -
Li, Jilong (MU-Student)