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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













1












$begingroup$


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?










share|improve this question









New contributor




solimanelefant is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
Check out our Code of Conduct.







$endgroup$







  • 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















1












$begingroup$


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?










share|improve this question









New contributor




solimanelefant is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
Check out our Code of Conduct.







$endgroup$







  • 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













1












1








1





$begingroup$


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?










share|improve this question









New contributor




solimanelefant is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
Check out our Code of Conduct.







$endgroup$




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






share|improve this question









New contributor




solimanelefant is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
Check out our Code of Conduct.











share|improve this question









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solimanelefant is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
Check out our Code of Conduct.









share|improve this question




share|improve this question








edited 2 days ago









Kamil S Jaron

3,057942




3,057942






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asked Apr 30 at 14:52









solimanelefantsolimanelefant

1083




1083




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New contributor





solimanelefant is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
Check out our Code of Conduct.






solimanelefant is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
Check out our Code of Conduct.







  • 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




    $begingroup$
    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










2 Answers
2






active

oldest

votes


















4












$begingroup$

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



  1. select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.


  2. Click on "Filters", and set Gene type to coding and Transcript type to protein_coding.


  3. From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".






share|improve this answer











$endgroup$




















    0












    $begingroup$

    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)





    share|improve this answer










    New contributor




    Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
    Check out our Code of Conduct.






    $endgroup$













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      2 Answers
      2






      active

      oldest

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      2 Answers
      2






      active

      oldest

      votes









      active

      oldest

      votes






      active

      oldest

      votes









      4












      $begingroup$

      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



      1. select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.


      2. Click on "Filters", and set Gene type to coding and Transcript type to protein_coding.


      3. From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".






      share|improve this answer











      $endgroup$

















        4












        $begingroup$

        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



        1. select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.


        2. Click on "Filters", and set Gene type to coding and Transcript type to protein_coding.


        3. From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".






        share|improve this answer











        $endgroup$















          4












          4








          4





          $begingroup$

          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



          1. select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.


          2. Click on "Filters", and set Gene type to coding and Transcript type to protein_coding.


          3. From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".






          share|improve this answer











          $endgroup$



          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



          1. select "Ensembl Genes 96" (the number will change if the version changes) as the database and "uman Genes" as the dataset.


          2. Click on "Filters", and set Gene type to coding and Transcript type to protein_coding.


          3. From "Attributes", select whatever you want to see. The "CDS Length" is under "Structures".







          share|improve this answer














          share|improve this answer



          share|improve this answer








          edited Apr 30 at 22:23

























          answered Apr 30 at 15:48









          terdonterdon

          4,9702830




          4,9702830





















              0












              $begingroup$

              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)





              share|improve this answer










              New contributor




              Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
              Check out our Code of Conduct.






              $endgroup$

















                0












                $begingroup$

                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)





                share|improve this answer










                New contributor




                Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
                Check out our Code of Conduct.






                $endgroup$















                  0












                  0








                  0





                  $begingroup$

                  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)





                  share|improve this answer










                  New contributor




                  Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
                  Check out our Code of Conduct.






                  $endgroup$



                  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)






                  share|improve this answer










                  New contributor




                  Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
                  Check out our Code of Conduct.









                  share|improve this answer



                  share|improve this answer








                  edited 2 days ago









                  Kamil S Jaron

                  3,057942




                  3,057942






                  New contributor




                  Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
                  Check out our Code of Conduct.









                  answered 2 days ago









                  Drew J-HDrew J-H

                  12




                  12




                  New contributor




                  Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
                  Check out our Code of Conduct.





                  New contributor





                  Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
                  Check out our Code of Conduct.






                  Drew J-H is a new contributor to this site. Take care in asking for clarification, commenting, and answering.
                  Check out our Code of Conduct.




















                      solimanelefant is a new contributor. Be nice, and check out our Code of Conduct.









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