User: wu.zhiqiang.1020
wu.zhiqiang.1020 • 20
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- United States
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- 7 months, 1 week ago
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- 5 years, 7 months ago
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Posts by wu.zhiqiang.1020
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... thanks, I find it and make it go through.
thanks again ...
written 15 months ago by
wu.zhiqiang.1020 • 20
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... It need other pm file to load and the same time.
I find this link. But I have to search other more pm files also
thanks
...
written 15 months ago by
wu.zhiqiang.1020 • 20
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... Dear all,
I want to filtered the Trinity outfile for RNAseq assemble. I know this is not the best choice, and there are some scripts online. but they are all not good to use in my data, Could you give me some suggestion on this?
my data like this: (Start with > for name)
>TRINITY_DN66086_c ...
written 15 months ago by
wu.zhiqiang.1020 • 20
• updated
15 months ago by
h.mon ♦ 15k
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... Hi st.ph.n
I tried your script, it shown error as
Traceback (most recent call last):
File "get_longest_iso.py", line 8, in
if line.startswith(">"):
NameError: name 'line' is not defined
could you help me to fix this? I do not know the python. thanks
My trinity out start as:
>TRI ...
written 15 months ago by
wu.zhiqiang.1020 • 20
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... thanks。 I need to read Trinity again.
...
written 15 months ago by
wu.zhiqiang.1020 • 20
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921
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... it would be helpful to keep the longest isoforms. but I still could not remove the duplicates from other contrig. right?
thanks
...
written 15 months ago by
wu.zhiqiang.1020 • 20
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... yes, I just want to have one longest isoform.
How can I realize that?
ZQ ...
written 15 months ago by
wu.zhiqiang.1020 • 20
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921
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... you mean -c and -t right?
...
written 15 months ago by
wu.zhiqiang.1020 • 20
0
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2
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921
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... Dear all,
I am trying to use CD-hit to remove the duplicates from the file that is the output from trinity (RNA seq assembly).
I used the following parameters:
cd-hit-est -i in.fasta -o out_cdhit90.fasta -c 0.90 -n 9 -d 0 -M 0 -T 0
But the output file still contains lots of small or fragmented s ...
written 15 months ago by
wu.zhiqiang.1020 • 20
• updated
15 months ago by
st.ph.n • 2.2k
0
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... I have a pooled RNA seq data from 5 to 10 individuals at different stages. I want to assemble them and combine all of data as one big fastq files. I use the bbnorm to reduce the replicates. But I have a question about how to set the parameters as:
target=100 (tgt) Target normalization ...
written 16 months ago by
wu.zhiqiang.1020 • 20
• updated
16 months ago by
genomax ♦ 49k
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