# How to convert fastqsanger to fasta

**URL:** <https://help.galaxyproject.org/t/how-to-convert-fastqsanger-to-fasta/1061>\
**Category:** usegalaxy.org support\
**Tags:** download, fastqgz, fastqsanger\
**Created:** [April 10, 2019, 5:58pm UTC](https://help.galaxyproject.org/t/how-to-convert-fastqsanger-to-fasta/1061 "2019-04-10T17:58:50Z")\
**Posts on this page:** 4\
**Page:** 1

<div class="post-metadata">

**Author:** ![OSIRIS](https://avatars.discourse-cdn.com/v4/letter/o/839c29/32.png) [@OSIRIS](https://help.galaxyproject.org/u/OSIRIS)\
**Post date:** [April 10, 2019, 5:58pm UTC](https://help.galaxyproject.org/t/how-to-convert-fastqsanger-to-fasta/1061/1 "2019-04-10T17:58:51Z")

</div>

Hello, i need my sequences in fastaq format, but when I split them (18s and 16s), galaxy gives me these in fastasanger format, and i dont know how to convert them.

---

<div class="post-metadata">

**Author:** ![jennaj](https://sea2.discourse-cdn.com/flex020/user_avatar/help.galaxyproject.org/jennaj/32/27_2.png) [@jennaj](https://help.galaxyproject.org/u/jennaj)\
**Post date:** [April 10, 2019, 11:17pm UTC](https://help.galaxyproject.org/t/how-to-convert-fastqsanger-to-fasta/1061/2 "2019-04-10T23:17:50Z")

</div>

Welcome, @OSIRIS!

I’m guessing that you need `FASTA` format? If yes, try the tool: `Convert Formats` \> `FASTQ to FASTA converter`.

If you instead need `FASTQ` format, the current format should be supported by the tool (if not, we would be curious about which is presenting with the input problem/rejection). `Fastqsanger` is a subtype of `FASTQ` format and, importantly, the subtype that is required by most Galaxy wrapped tools.

FAQs (with more here: [https://galaxyproject.org/support](https://galaxyproject.org/support))

- [Common datatypes explained](https://galaxyproject.org/learn/datatypes/)

If that doesn’t help, please explain more about your goals/inputs.

Thanks!

---

<div class="post-metadata">

**Author:** ![OSIRIS](https://avatars.discourse-cdn.com/v4/letter/o/839c29/32.png) [@OSIRIS](https://help.galaxyproject.org/u/OSIRIS)\
**Post date:** [April 11, 2019, 2:48am UTC](https://help.galaxyproject.org/t/how-to-convert-fastqsanger-to-fasta/1061/3 "2019-04-11T02:48:31Z")

</div>

Thanks jennaj, I was so happy cause I found in Galaxy a way to convert my sequences in format fastq.gz when I splitted them into 16s and 18s. But my file didn’t work; my sequences looks good in galaxy plataform (fast.gz), but winrar, winzip, 7z couldn’t open, I don’t know why ☹ it said that my file is damage.

---

<div class="post-metadata">

**Author:** ![jennaj](https://sea2.discourse-cdn.com/flex020/user_avatar/help.galaxyproject.org/jennaj/32/27_2.png) [@jennaj](https://help.galaxyproject.org/u/jennaj)\
**Post date:** [April 11, 2019, 1:22pm UTC](https://help.galaxyproject.org/t/how-to-convert-fastqsanger-to-fasta/1061/4 "2019-04-11T13:22:18Z")

</div>

It sounds like the `.gz` compression is not compatible for some reason. Uncompress the data in Galaxy, then download it in that format. You can always compress again using Window tools after.

Use `curl` or `wget` to get larger datasets. FAQ: [Downloading Data](https://galaxyproject.org/support/download-data/)
