You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Sorry again for ask this question here because I can not find a issue page or your email in the stringtie2 page. You can close this issue whenever you like.
From your paper about stringtie2, I believe i can handle my Ont RNA reads well with it.
But I get a much larger transcripts(about 30-40k) from stringtie2 no matter use ONT reads or Illumina reads., but the actually length should be 3-4k. I did all these with default paras and the input bam all result from hisat and minimap2.
Could you please give some tips about this or How should I process my Ont reads for genome annotation.
Thanks a lot.
ZhangZhou from JXAU,Nanchang,China.
The text was updated successfully, but these errors were encountered:
Hello, Dr Skovaka:
Sorry again for ask this question here because I can not find a issue page or your email in the stringtie2 page. You can close this issue whenever you like.
From your paper about stringtie2, I believe i can handle my Ont RNA reads well with it.
But I get a much larger transcripts(about 30-40k) from stringtie2 no matter use ONT reads or Illumina reads., but the actually length should be 3-4k. I did all these with default paras and the input bam all result from hisat and minimap2.
Could you please give some tips about this or How should I process my Ont reads for genome annotation.
Thanks a lot.
ZhangZhou from JXAU,Nanchang,China.
The text was updated successfully, but these errors were encountered: