Comments (5)
Hello @jamesboot
A few things I would test out.
I think it might be because this version doesn't check for 0 counts and I think this is what is happening there.
- Are you sure about the UMI stopping at 16bp? Not super important, but it might give you a little increase in your UMI counts depending on your library's diversity and its size.
- Can you run the same without the whitelist? I suspect There is no cell barcode overlap. This usually happens on SCv3 from 10x runs.
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Hi Patrick,
Thanks very much for your quick response. I tried running without the whitelist (all other options the same as above) but still got the same error message:
Correcting umis
Traceback (most recent call last):
File "/data/home/hmy961/citeseq-counts-env/bin/CITE-seq-Count", line 8, in <module>
sys.exit(main())
File "/data/home/hmy961/citeseq-counts-env/lib/python3.8/site-packages/cite_seq_count/__main__.py", line 603, in main
io.write_dense(
File "/data/home/hmy961/citeseq-counts-env/lib/python3.8/site-packages/cite_seq_count/io.py", line 48, in write_dense
pandas_dense = pd.DataFrame(sparse_matrix.todense(), columns=columns, index=index)
File "/data/home/hmy961/citeseq-counts-env/lib/python3.8/site-packages/pandas/core/frame.py", line 639, in __init__
raise ValueError("columns cannot be a set")
ValueError: columns cannot be a set
I'm pretty sure the UMI stops at 16bp. We are using 10X 5' v2 chemistry if that helps.
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I think this is a bug with the newest pandas version: facebook/Ax#1153
Can you try to reinstall with pandas 1.4?
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I think this is a bug with the newest pandas version: facebook/Ax#1153
Can you try to reinstall with pandas 1.4?
This fixed the error for me. I think it's because, in pandas 1.5, they no longer allow DataFrame columns to be set by a set datatype. io.py has a line that creates a DataFrame by setting the columns with a set datatype.
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Sorry for taking some time to come back to this. Running with pandas 1.4 fixed the problem for me too! Thanks for your help!
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Related Issues (20)
- Different "UMIs corrected" results between v1.4.3 and v1.4.5 HOT 2
- Code for running multiple lanes
- Python error when there are too many cells? Script never finishes HOT 2
- Cell Hashing on Multiome samples HOT 11
- bug in preprocessing.py -> get_read_paths() (version 1.4.3) HOT 1
- method keeps looking for whitelist when not provided. HOT 8
- 100% unmapped
- Discussion question -- is it normal to take so long? HOT 3
- Include path to tag file in run report HOT 1
- barcodes with 0s in all protein tags and unmapped roll HOT 2
- Running Cite-Seq-count with next GEM protocol HOT 2
- Pandas error after correcting UMIs HOT 1
- Allow to split fastq or get list of readID per cell HOT 2
- Unable to locate temp file while merging results
- Does not compile using Python version > 3.9.x please fix.
- Gene and Antibody both have a pair of fastq files, how to run CITE-seq-Count?
- Please, trim all sequences at the same length.
- CITE-seq-Count run gets stuck
- ValueError: columns cannot be a set HOT 3
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