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Fast alignment and preprocessing of chromatin profiles

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Hi, Thanks for the great software. I've been running chromap (`-preset atac -t 8`, otherwise default params) on a lot of samples from the literature, but I'm getting 'core dumped'...

bug

Hello @haowenz: 1. I am wondering how `chromap` handel Hi-C without knowing the information of restriction enzyme? 2. I am testing `chromap` with a Hi-C library using combination of two...

I am trying to map chipseq data, without providing a barcode file. chromap fails after mapping with the following error: ``` Numbers of reads and barcodes don't match! ``` Does...

Hi~ Thanks for the useful software! Are you considering adding score and Beto the bed file output from single cell ATAC mode? Best, Yumo Song

Hi all, I understand SAM output is not optimized and it is discouraged, however I had to test it and I run into some issues. First of all, output is...

enhancement

``` ❯ chromap --version 0.1-r208 ❯ which igv.sh ~/IGV_Linux_2.8.12/igv.sh ``` When loading the chromap-mapped(0.1-r208) paried-ended bam file to IGV ( version :Linux 2.8.12 ), the forward reads display fine, but...

bug

Hi, We have mapped our illumina short reads to our genome using typical commands with --SAM of chromap. ![45b8ab262cb63858d73611e96de4d93](https://user-images.githubusercontent.com/49976278/127955610-04cd37bd-4bae-4cb0-ad1e-d2a1c492e90e.png) But I failed to find the tag like "NH:i:" or "XT:A:U"...

Hi, is there any way to force chromap to output all the unmapped and multi-mapped reads? And how are they identified? It was mentioned in issue 20 that multi-mapped reads...

Ciao ! On a fresh MAESTRO — release 1.5.1 — installation (Ubuntu 18.04 with Python v3.8.12 installed) I tried to run chromap, chromap --version or chromap -h having immediately Illegal...

I'm aligning 10x genomics scATAC-seq to the rheMac10 genome. The sequencing is 50bp for R1 and R2 paired-end sequencing on the Novaseq. The genome was built with k`17` and w`7`...

documentation
enhancement