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Hi,
Hope that seqkit can extract transrcipt/cdna/gene/protein sequences from references fasta and gff/gtf file. gffread can do this but it can not handle large chromosomes correctly.
Best,
Kun
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**Describe the bug**
When using the Electra model for POS for sequences longer than a specific number of tokens (varies with language), the forward method of the Electra model throws an incompatible …
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Hi, I am using the latest version 0.13, and when mapping reads against co-assembled contigs, no sam file is created. This message appears in the log file:
This is strobealign 0.13.0
Estimated rea…
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Can we add the primers for SSR and RFLP markers to the records in GlycineMine? Example Satt430 does not present the primer sequences just the motif. This might also be a datastore issue? @adf-ncgr @S…
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Dear author, the tool you compiled is a very great tool for protein function prediction, very useful for my research, but in the big_space step of the process my genome will encounter I encountered an…
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I notice that idlc generates `__alloc()` and `_free()` functions for constructed types but does not generate a function for deep copying.
Deep copy functions would make life easier when programming i…
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Reported by Toby
The genome sequence displayed in the "Reference sequence" track is completely different to that displayed in the "Annotations" track (or more accurately out of sync with each by a …
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I have a fasta file containing several sequences. By default quadron concatenates these sequences. Is there any way to avoid it receive a score for each sequence?
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Hiya，
When I run `snakemake -j 64 --use-conda` with example data, I ran into this error:
localrule antismash:
input: intermediate_files/annot/syringae_UMAF1029_O/Pseudomonas_syringae_UMAF1029…
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一装插件就这样了
2024-11-01 14:54:09 E/main: Failed to init MiraiConsole.
net.mamoe.mirai.console.internal.util.ServiceLoadException: Could not load service xyz.cssxsh.mirai.skia.MiraiSkiaPlugin.
at net.ma…