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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

Broken GATK4 documentation links

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    Gökalp Çelik

    Hi Steffen Møller Bøttger

    This has been a known issue and we are working on getting it resolved. Some of those links were remnants of the old version of the zendesk that we are using and new zendesk migration clearly changed the way those articles are indexed in an unexpected way and we are getting to update our links.

    Can you point me towards the actual article that you find this link on? I will see what the problem is and fix it if it is an easy one. 

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    Steffen Møller Bøttger

    Dear Gökalp Çelik

    Thank you for looking into this. The article containing the mentioned link can be found here:

    https://gatk.broadinstitute.org/hc/en-us/articles/21905025322523-HaplotypeCaller

    There are several links in the article having the issue, though. The specific link, I referred to is tied to the word "here", which is the last word in the final paragraph before the following headline:

    How HaplotypeCaller works

    After this headline, there are four numbered headlines that are also links that have the issue. Furthermore, there is a problematic link tied to the words "allele-specific annotations", a problematic link tied to the word "bamout", and finally a problematic link tied to the words "this document" in the last bullet under Additional Notes.

    So for this article alone, I found eight broken links - I imagine it cannot be a small task to fix such issues throughout the site. Would it be a help to you if we, the grateful users, would continue to send you feedback when we come across such broken links? Thank you.

    Best, Steffen 

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    Gökalp Çelik

    Hi again. These documentation links are tied to the GATK source code directly thus compiled during the time of release. Thank you for indicating this issue here. We will update the source code with proper links and new release will sure contain proper links directly. 

    For the link you mentioned in the first part is related to RNAseq variant calling best practices document from a distant past but we have a newer version in the making and you can consult to that one 

    https://gatk.broadinstitute.org/hc/en-us/articles/360035531192-RNAseq-short-variant-discovery-SNPs-Indels 

    In summary STAR aligned reads should be processed with our tool SplitNCigarReads to be compatible with HaplotypeCaller to perform its function. 

    I hope this helps.

    Regards. 

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    Steffen Møller Bøttger

    Thank you very much!

    Regards

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