Open naglem opened 7 years ago
Hi Michael, The error message suggests an issue with reading Franke.ldcts (or ImmGen.ldcts), specifically that it’s hitting a line that doesn’t have the expected two fields.
I haven’t been able to replicate the error yet. The line reporting the error parses Franke.ldcts without any issues for me. I’m in the process of a full test run with the Franke data, but it has made it past the point where this error should arise and is still running smoothly.
Have you done anything to modify the .ldcts files? On the small chance Franke.ldcts somehow got corrupted, could you try redownloading that file and rerunning?
Cheers, Raymond
On May 15, 2017, at 4:20 PM, Michael Nagle notifications@github.com wrote:
Hi,
I've successfully replicated results using some of the ldscores from the most recent biorxiv paper for partitioned heritability (Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types) including the gtex and cahoy annotations. However, I run into the same error for the Franke and ImmGen data: line 286, in cell_type_specific for (name, ct_ld_chr) in [x.split() for x in open(args.ref_ld_chr_cts).readlines()]: ValueError: need more than 0 values to unpack Any help on this would be great, thanks.
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Thanks, I did modify the .ldcts files to reflect my paths. I went back and reformatted them again, and works like a charm.
Thanks for the assist.
Hi,
I've successfully replicated results using some of the ldscores from the most recent biorxiv paper for partitioned heritability (Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types) including the gtex and cahoy annotations. However, I run into the same error for the Franke and ImmGen data: line 286, in cell_type_specific for (name, ct_ld_chr) in [x.split() for x in open(args.ref_ld_chr_cts).readlines()]: ValueError: need more than 0 values to unpack Any help on this would be great, thanks.