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Dear brocklab research group:
You did an excellent job in the field of lineage-tracing. Our research group is using the technology you developed to construct the ClonMapper library.In or…
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現在 v0.2.2 のREADMEにあるExampleについて、出力の説明を加えてください。
https://github.com/aki2274/KOnezumi-AID?tab=readme-ov-file#examples-1
具体的には、以下の質問が想定されますので、こちらに答えられるような説明をいれるとよいのかと思っております👀
- `gene symbol`で得られた…
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I am trying to test SBOL converter to convert genbank files to SBOL.
I keeps flagging the following error:
Converting GenBank to SBOL Version 2
TopLevel https://synbiohub.org/user/gbaldwin/…
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### To Be
- ガイドの配列情報からすぐにCRISPRdirectにアクセスできるようにする.
- ガイドがどのアミノ酸を標的としているか表示させる.(ファーストステップとしてはWを狙っているかを表示させる.)
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HI,
I just found this other tool after having found first DNABarcodeCompatibility
Could you please comment about this tool and my ticket present there
https://github.com/comoto-pasteur-fr/DNABa…
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Hello everyone,
I am here in search of help to know the tool mageck better a s I am facing problem in allignling my reads on library file. ZerosgRNA is having 0 count. Can you help me in this??
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### As Is(今の状態を記載)
いまのREADMEにある出力(一部)は以下のようになっております。
```text
PTC gRNA
seq in_start_150bp in_50bp_from_LEJ
0 ACAGTTTGGCGGCGTTCGGGTGG True Fal…
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Hi, thank you so much for developing this fantastic MAGeCK package, its really helpful in analysing CRISPR-screen data. However, I am facing issues when I try to analyse the data using the paired end …
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Hi @ofiryaish ,
thank you and your colleagues for developing this valuable tool for the community.
I'd love to give it a go. But I ran into errors.
The command I used:
'''
java -cp bin Smi…
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I am training nanoGPT on a dataset with ~800,000 COVID-19 research papers on an A100 GPU.
```
--n_layer=48 --n_head=8 --n_embd=64 --device='cuda' --compile=False --eval_iters=1 --block_size=2048 --b…