Closed mgsrod closed 1 year ago
Hi Rod,
Is your data single end ?
Best, Simon
Hi Simon, Thanks for getting back to me so soon. Yes, its single end data.
Hi Simon,
Yes, it’s single end data
Rod Eyles, PhD Post Doctoral Researcher, Microbial Genomics & Symbiosis Lab @.***
Instituto Gulbenkian de Ciência Rua da Quinta Grande 6 2780-156 Oeiras, Portugal Website https://gulbenkian.pt/ciencia/ | Facebook https://www.facebook.com/InstitutoGulbenkianCiencia | Instagram https://www.instagram.com/igciencia/?hl=en | Twitter https://twitter.com/igciencia | LinkedIn https://www.linkedin.com/company/instituto-gulbenkian-de-ciencia/
On 6 Feb 2023, at 12:11 pm, Simon-Leonard @.***> wrote:
Hi Rod,
Is your data single end ?
Best, Simon
— Reply to this email directly, view it on GitHub https://github.com/Simon-Leonard/APERO/issues/10#issuecomment-1418982835, or unsubscribe https://github.com/notifications/unsubscribe-auth/A4THXWLML5FXDQOHBKTPQ2TWWDS6XANCNFSM6AAAAAAUSSEOKA. You are receiving this because you authored the thread.
Initially APERO was not dedicated to work on single end data but I had some requests so I created a separated branch in github. Can you try the procedure mentionned in https://github.com/Simon-Leonard/APERO/issues/3#issuecomment-605458633 ? You just have to install a particular branch and add a parameter to the functions.
Simon
Hi, I receive the following error when I attempt to run APERO:
My input is as follows:b. APERO_start_detection(work_dir = ("/apero"), bam_name = "sortedbam.bam", ptt_file = NULL, wmax = 10, min_dist = 10, enrichment = 0.1, min_read_number = 0, genome_size = 2000000)
APERO is working with the sample data using the same options.
My BAM file is sorted and seems complete: @HD VN:1.0 SO:coordinate @SQ SN:KQ033870.1 LN:107658 @SQ SN:KQ033871.1 LN:2001565 @SQ SN:KQ033872.1 LN:3680 @SQ SN:KQ033873.1 LN:1903 @SQ SN:KQ033874.1 LN:1484 @SQ SN:KQ033875.1 LN:1478 @SQ SN:KQ033876.1 LN:610 @PG ID:bowtie2 PN:bowtie2 VN:2.2.5
Any ideas on how to fix this issue?
All the best,
Rod