CDS length for each human geneIs there a way to retrieve ENSEMBL IDs from a search query?Converting Ensembl Gene IDs to Entrez Gene IDs through biomartIdentifying relevant SNPs from a listCounting the number of paralogues for mouse genes gives me the wrong frequency in RA good tool for gene locus visualizationDownload proteomes from NCBI based only on binomial namesGet Gene Expression Matrix from GEOqueryFinding gene length using ensembl IDFinding gene name from human genome using SP1 transcrition factor binding site from Postion Weight MatrixRetrieve RNA sequencing data for human p53 colon cancer cell lines
Formatting Datetime.now()
Would a small hole in a Faraday cage drastically reduce its effectiveness at blocking interference?
What was Bran's plan to kill the Night King?
Why do people keep telling me that I am a bad photographer?
Can I use a Cat5e cable with an RJ45 and Cat6 port?
What is a common way to tell if an academic is "above average," or outstanding in their field? Is their h-index (Hirsh index) one of them?
How to deal with employer who keeps me at work after working hours
Start job from another SQL server instance
How does summation index shifting work?
Is there precedent or are there procedures for a US president refusing to concede to an electoral defeat?
What are the advantages of luxury car brands like Acura/Lexus over their sibling non-luxury brands Honda/Toyota?
Mug and wireframe entirely disappeared
Why is "breaking the mould" positively connoted?
Trigonometry substitution issue with sign
Handling Null values (and equivalents) routinely in Python
Will 700 more planes a day fly because of the Heathrow expansion?
Is there a word that describes the unjustified use of a more complex word?
Does "Captain Marvel" contain spoilers for "Avengers: Infinity War"?
What do I do if my advisor made a mistake?
Find magical solution to magical equation
Are the Night's Watch still required?
Checking if two expressions are related
Why would a military not separate its forces into different branches?
Out of scope work duties and resignation
CDS length for each human gene
Is there a way to retrieve ENSEMBL IDs from a search query?Converting Ensembl Gene IDs to Entrez Gene IDs through biomartIdentifying relevant SNPs from a listCounting the number of paralogues for mouse genes gives me the wrong frequency in RA good tool for gene locus visualizationDownload proteomes from NCBI based only on binomial namesGet Gene Expression Matrix from GEOqueryFinding gene length using ensembl IDFinding gene name from human genome using SP1 transcrition factor binding site from Postion Weight MatrixRetrieve RNA sequencing data for human p53 colon cancer cell lines
$begingroup$
Does anyone know where and how could I download a list of all human genes and the length of the coding sequence for each gene? Is it possible to do this on the NCBI site, ensembl?
gene sequence-analysis ncbi ensembl
New contributor
$endgroup$
add a comment |
$begingroup$
Does anyone know where and how could I download a list of all human genes and the length of the coding sequence for each gene? Is it possible to do this on the NCBI site, ensembl?
gene sequence-analysis ncbi ensembl
New contributor
$endgroup$
2
$begingroup$
Which coding sequence? I mean, do you just want whichever has been designated the 'canonical' transcript or do you want all possible isoforms?
$endgroup$
– terdon♦
Apr 30 at 14:54
$begingroup$
Hi terdon, thanks for the quick reply! Yes exactly, the canonical transcript is good enough!
$endgroup$
– solimanelefant
Apr 30 at 14:56
1
$begingroup$
Michael G. suggests to take a look at relevant front-end, NCBI's eFetch. Which is supposedly perfect for what you need.
$endgroup$
– Kamil S Jaron
2 days ago
add a comment |
$begingroup$
Does anyone know where and how could I download a list of all human genes and the length of the coding sequence for each gene? Is it possible to do this on the NCBI site, ensembl?
gene sequence-analysis ncbi ensembl
New contributor
$endgroup$
Does anyone know where and how could I download a list of all human genes and the length of the coding sequence for each gene? Is it possible to do this on the NCBI site, ensembl?
gene sequence-analysis ncbi ensembl
gene sequence-analysis ncbi ensembl
New contributor
New contributor
edited 2 days ago
Kamil S Jaron
3,057942
3,057942
New contributor
asked Apr 30 at 14:52
solimanelefantsolimanelefant
1083
1083
New contributor
New contributor
2
$begingroup$
Which coding sequence? I mean, do you just want whichever has been designated the 'canonical' transcript or do you want all possible isoforms?
$endgroup$
– terdon♦
Apr 30 at 14:54
$begingroup$
Hi terdon, thanks for the quick reply! Yes exactly, the canonical transcript is good enough!
$endgroup$
– solimanelefant
Apr 30 at 14:56
1
$begingroup$
Michael G. suggests to take a look at relevant front-end, NCBI's eFetch. Which is supposedly perfect for what you need.
$endgroup$
– Kamil S Jaron
2 days ago
add a comment |
2
$begingroup$
Which coding sequence? I mean, do you just want whichever has been designated the 'canonical' transcript or do you want all possible isoforms?
$endgroup$
– terdon♦
Apr 30 at 14:54
$begingroup$
Hi terdon, thanks for the quick reply! Yes exactly, the canonical transcript is good enough!
$endgroup$
– solimanelefant
Apr 30 at 14:56
1
$begingroup$
Michael G. suggests to take a look at relevant front-end, NCBI's eFetch. Which is supposedly perfect for what you need.
$endgroup$
– Kamil S Jaron
2 days ago
2
2
$begingroup$
Which coding sequence? I mean, do you just want whichever has been designated the 'canonical' transcript or do you want all possible isoforms?
$endgroup$
– terdon♦
Apr 30 at 14:54
$begingroup$
Which coding sequence? I mean, do you just want whichever has been designated the 'canonical' transcript or do you want all possible isoforms?
$endgroup$
– terdon♦
Apr 30 at 14:54
$begingroup$
Hi terdon, thanks for the quick reply! Yes exactly, the canonical transcript is good enough!
$endgroup$
– solimanelefant
Apr 30 at 14:56
$begingroup$
Hi terdon, thanks for the quick reply! Yes exactly, the canonical transcript is good enough!
$endgroup$
– solimanelefant
Apr 30 at 14:56
1
1
$begingroup$
Michael G. suggests to take a look at relevant front-end, NCBI's eFetch. Which is supposedly perfect for what you need.
$endgroup$
– Kamil S Jaron
2 days ago
$begingroup$
Michael G. suggests to take a look at relevant front-end, NCBI's eFetch. Which is supposedly perfect for what you need.
$endgroup$
– Kamil S Jaron
2 days ago
add a comment |
2 Answers
2
active
oldest
votes
$begingroup$
While I haven't found a way to limit the results to the canonical transcript only, you can get a list of genes, transcripts and their CDS lengths using Ensemble's BioMart. I have already set it up for you, you can see the results, and modify them, here (click on the "Results" link if you don't see them).
Essentially, you just need to go to BioMart, and
select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.
Click on "Filters", and set
Gene type
tocoding
andTranscript type
toprotein_coding
.From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".
$endgroup$
add a comment |
$begingroup$
Ensembl has an FTP site that allows you to select and download only the coding sequences from many different genomes.
https://useast.ensembl.org/info/data/ftp/index.html
To determine the length of those sequences, download the associated gtf or gff3 annotation file. The annotation file is tab delim. The fourth and fifth column represent genomic loci of the annotated region. Subtract the amount in the fourth column from the amount in the fifth column to yield the length of all the annotated features.
You can easily do this in R after loading the file in the environment using the Magrittr library. The following code will create a new column called gene_length with the associated gene lengths.
install.packages("magrittr")
# this only needs to be done once
library(magrittr)
# must be run each time the library is neaded
annotation.gtf <- read.table("path/to/annotation.gtf")
annotation.gtf$start <- annotation.gtf[,4]
annotation.gtf$end <- annotation.gtf[,5]
annotation.new-column.gtf <- annotation.gtf %>%
mutate(gene_length=end-start)
New contributor
$endgroup$
add a comment |
Your Answer
StackExchange.ready(function()
var channelOptions =
tags: "".split(" "),
id: "676"
;
initTagRenderer("".split(" "), "".split(" "), channelOptions);
StackExchange.using("externalEditor", function()
// Have to fire editor after snippets, if snippets enabled
if (StackExchange.settings.snippets.snippetsEnabled)
StackExchange.using("snippets", function()
createEditor();
);
else
createEditor();
);
function createEditor()
StackExchange.prepareEditor(
heartbeatType: 'answer',
autoActivateHeartbeat: false,
convertImagesToLinks: false,
noModals: true,
showLowRepImageUploadWarning: true,
reputationToPostImages: null,
bindNavPrevention: true,
postfix: "",
imageUploader:
brandingHtml: "Powered by u003ca class="icon-imgur-white" href="https://imgur.com/"u003eu003c/au003e",
contentPolicyHtml: "User contributions licensed under u003ca href="https://creativecommons.org/licenses/by-sa/3.0/"u003ecc by-sa 3.0 with attribution requiredu003c/au003e u003ca href="https://stackoverflow.com/legal/content-policy"u003e(content policy)u003c/au003e",
allowUrls: true
,
onDemand: true,
discardSelector: ".discard-answer"
,immediatelyShowMarkdownHelp:true
);
);
solimanelefant is a new contributor. Be nice, and check out our Code of Conduct.
Sign up or log in
StackExchange.ready(function ()
StackExchange.helpers.onClickDraftSave('#login-link');
);
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
StackExchange.ready(
function ()
StackExchange.openid.initPostLogin('.new-post-login', 'https%3a%2f%2fbioinformatics.stackexchange.com%2fquestions%2f8552%2fcds-length-for-each-human-gene%23new-answer', 'question_page');
);
Post as a guest
Required, but never shown
2 Answers
2
active
oldest
votes
2 Answers
2
active
oldest
votes
active
oldest
votes
active
oldest
votes
$begingroup$
While I haven't found a way to limit the results to the canonical transcript only, you can get a list of genes, transcripts and their CDS lengths using Ensemble's BioMart. I have already set it up for you, you can see the results, and modify them, here (click on the "Results" link if you don't see them).
Essentially, you just need to go to BioMart, and
select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.
Click on "Filters", and set
Gene type
tocoding
andTranscript type
toprotein_coding
.From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".
$endgroup$
add a comment |
$begingroup$
While I haven't found a way to limit the results to the canonical transcript only, you can get a list of genes, transcripts and their CDS lengths using Ensemble's BioMart. I have already set it up for you, you can see the results, and modify them, here (click on the "Results" link if you don't see them).
Essentially, you just need to go to BioMart, and
select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.
Click on "Filters", and set
Gene type
tocoding
andTranscript type
toprotein_coding
.From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".
$endgroup$
add a comment |
$begingroup$
While I haven't found a way to limit the results to the canonical transcript only, you can get a list of genes, transcripts and their CDS lengths using Ensemble's BioMart. I have already set it up for you, you can see the results, and modify them, here (click on the "Results" link if you don't see them).
Essentially, you just need to go to BioMart, and
select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.
Click on "Filters", and set
Gene type
tocoding
andTranscript type
toprotein_coding
.From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".
$endgroup$
While I haven't found a way to limit the results to the canonical transcript only, you can get a list of genes, transcripts and their CDS lengths using Ensemble's BioMart. I have already set it up for you, you can see the results, and modify them, here (click on the "Results" link if you don't see them).
Essentially, you just need to go to BioMart, and
select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.
Click on "Filters", and set
Gene type
tocoding
andTranscript type
toprotein_coding
.From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".
edited Apr 30 at 22:23
answered Apr 30 at 15:48
terdon♦terdon
4,9702830
4,9702830
add a comment |
add a comment |
$begingroup$
Ensembl has an FTP site that allows you to select and download only the coding sequences from many different genomes.
https://useast.ensembl.org/info/data/ftp/index.html
To determine the length of those sequences, download the associated gtf or gff3 annotation file. The annotation file is tab delim. The fourth and fifth column represent genomic loci of the annotated region. Subtract the amount in the fourth column from the amount in the fifth column to yield the length of all the annotated features.
You can easily do this in R after loading the file in the environment using the Magrittr library. The following code will create a new column called gene_length with the associated gene lengths.
install.packages("magrittr")
# this only needs to be done once
library(magrittr)
# must be run each time the library is neaded
annotation.gtf <- read.table("path/to/annotation.gtf")
annotation.gtf$start <- annotation.gtf[,4]
annotation.gtf$end <- annotation.gtf[,5]
annotation.new-column.gtf <- annotation.gtf %>%
mutate(gene_length=end-start)
New contributor
$endgroup$
add a comment |
$begingroup$
Ensembl has an FTP site that allows you to select and download only the coding sequences from many different genomes.
https://useast.ensembl.org/info/data/ftp/index.html
To determine the length of those sequences, download the associated gtf or gff3 annotation file. The annotation file is tab delim. The fourth and fifth column represent genomic loci of the annotated region. Subtract the amount in the fourth column from the amount in the fifth column to yield the length of all the annotated features.
You can easily do this in R after loading the file in the environment using the Magrittr library. The following code will create a new column called gene_length with the associated gene lengths.
install.packages("magrittr")
# this only needs to be done once
library(magrittr)
# must be run each time the library is neaded
annotation.gtf <- read.table("path/to/annotation.gtf")
annotation.gtf$start <- annotation.gtf[,4]
annotation.gtf$end <- annotation.gtf[,5]
annotation.new-column.gtf <- annotation.gtf %>%
mutate(gene_length=end-start)
New contributor
$endgroup$
add a comment |
$begingroup$
Ensembl has an FTP site that allows you to select and download only the coding sequences from many different genomes.
https://useast.ensembl.org/info/data/ftp/index.html
To determine the length of those sequences, download the associated gtf or gff3 annotation file. The annotation file is tab delim. The fourth and fifth column represent genomic loci of the annotated region. Subtract the amount in the fourth column from the amount in the fifth column to yield the length of all the annotated features.
You can easily do this in R after loading the file in the environment using the Magrittr library. The following code will create a new column called gene_length with the associated gene lengths.
install.packages("magrittr")
# this only needs to be done once
library(magrittr)
# must be run each time the library is neaded
annotation.gtf <- read.table("path/to/annotation.gtf")
annotation.gtf$start <- annotation.gtf[,4]
annotation.gtf$end <- annotation.gtf[,5]
annotation.new-column.gtf <- annotation.gtf %>%
mutate(gene_length=end-start)
New contributor
$endgroup$
Ensembl has an FTP site that allows you to select and download only the coding sequences from many different genomes.
https://useast.ensembl.org/info/data/ftp/index.html
To determine the length of those sequences, download the associated gtf or gff3 annotation file. The annotation file is tab delim. The fourth and fifth column represent genomic loci of the annotated region. Subtract the amount in the fourth column from the amount in the fifth column to yield the length of all the annotated features.
You can easily do this in R after loading the file in the environment using the Magrittr library. The following code will create a new column called gene_length with the associated gene lengths.
install.packages("magrittr")
# this only needs to be done once
library(magrittr)
# must be run each time the library is neaded
annotation.gtf <- read.table("path/to/annotation.gtf")
annotation.gtf$start <- annotation.gtf[,4]
annotation.gtf$end <- annotation.gtf[,5]
annotation.new-column.gtf <- annotation.gtf %>%
mutate(gene_length=end-start)
New contributor
edited 2 days ago
Kamil S Jaron
3,057942
3,057942
New contributor
answered 2 days ago
Drew J-HDrew J-H
12
12
New contributor
New contributor
add a comment |
add a comment |
solimanelefant is a new contributor. Be nice, and check out our Code of Conduct.
solimanelefant is a new contributor. Be nice, and check out our Code of Conduct.
solimanelefant is a new contributor. Be nice, and check out our Code of Conduct.
solimanelefant is a new contributor. Be nice, and check out our Code of Conduct.
Thanks for contributing an answer to Bioinformatics Stack Exchange!
- Please be sure to answer the question. Provide details and share your research!
But avoid …
- Asking for help, clarification, or responding to other answers.
- Making statements based on opinion; back them up with references or personal experience.
Use MathJax to format equations. MathJax reference.
To learn more, see our tips on writing great answers.
Sign up or log in
StackExchange.ready(function ()
StackExchange.helpers.onClickDraftSave('#login-link');
);
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
StackExchange.ready(
function ()
StackExchange.openid.initPostLogin('.new-post-login', 'https%3a%2f%2fbioinformatics.stackexchange.com%2fquestions%2f8552%2fcds-length-for-each-human-gene%23new-answer', 'question_page');
);
Post as a guest
Required, but never shown
Sign up or log in
StackExchange.ready(function ()
StackExchange.helpers.onClickDraftSave('#login-link');
);
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
Sign up or log in
StackExchange.ready(function ()
StackExchange.helpers.onClickDraftSave('#login-link');
);
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
Sign up or log in
StackExchange.ready(function ()
StackExchange.helpers.onClickDraftSave('#login-link');
);
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Sign up using Google
Sign up using Facebook
Sign up using Email and Password
Post as a guest
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
Required, but never shown
2
$begingroup$
Which coding sequence? I mean, do you just want whichever has been designated the 'canonical' transcript or do you want all possible isoforms?
$endgroup$
– terdon♦
Apr 30 at 14:54
$begingroup$
Hi terdon, thanks for the quick reply! Yes exactly, the canonical transcript is good enough!
$endgroup$
– solimanelefant
Apr 30 at 14:56
1
$begingroup$
Michael G. suggests to take a look at relevant front-end, NCBI's eFetch. Which is supposedly perfect for what you need.
$endgroup$
– Kamil S Jaron
2 days ago