User: karthic

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karthic100
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Posts by karthic

<prev • 52 results • page 1 of 6 • next >
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Comment: C: Creating interaction network using cytoscape
... Hi Piyush, you can study PPI using ClusterOne. First submit your proteins to Sting DB and fetch the interaction table. Then submit the interaction table to Cytoscape and run ClusterOne on that. Sample input is below.. node1 interaction node2 combined_score DappuP317081 combined_score Dap ...
written 23 days ago by karthic100
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Comment: C: What is Genome-sequencing?
... I believe the user has copied the text from a manuscript and pasted here and trying to figure out the term "Genome Sequencing" in that text mean!! ...
written 27 days ago by karthic100
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Comment: C: target gene selection for miRNA
... Sorry that answer was for miRanda output. For targetscan you can select the ones which have low total context++ scores. KK ...
written 27 days ago by karthic100
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Comment: C: num_threads with blastn in blast 2.6.0+
... Ofcourse several times. Here is the sample command.. > blastn -query query_sequence.fa -db /blastdb/nr -evalue 0.0001 -outfmt > "6 qseqid sseqid pident qlen length mismatch gapope evalue bitscore > qcovs" -out blast_output.txt -perc_identity 100.00 -num_threads 5 ...
written 27 days ago by karthic100
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Comment: C: target gene selection for miRNA
... Hi, You can filter the targetscan results by selecting the ones having energy threshold less than -20 Kcal/mol. Also check the percentage coverage of your query and you can filter based upon them too. KK ...
written 27 days ago by karthic100
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Comment: C: Creating interaction network using cytoscape
... Hi, You can add ClusterOne app to the Cytoscape and do the cluster analysis and plot the interaction map KK ...
written 28 days ago by karthic100
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Comment: C: num_threads with blastn in blast 2.6.0+
... It may not use all the threads allocated by you. However it uses multiple threads according to its requirement. KK ...
written 28 days ago by karthic100
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Answer: A: Coloring nodes by tip label attribute in figtree
... Hi, Why dont you try itol [https://itol.embl.de/], it is easy and you can choose whatever color you want, KK ...
written 8 weeks ago by karthic100
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Comment: C: Protein Structure and Sequence Assessment
... It sounds like you want to do homology modelling of your sequences. There is an online tool called Rampage, which will give ramachandran plot for your predicted structure and gives the percentage of amino acids present in outlier regions etc. Also you have an online tool called Prosa, which will c ...
written 8 weeks ago by karthic100
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Comment: C: How do I study a drug target (Thioredoxin Reductase) in Giardia using data from
... First you need to study about that enzyme, and know its complete pathway and identify how it can be targeted. Find out its active sites. Then from literature or database such as chembl you can identify possible compounds which can target that enzyme. And later probable you can go for docking, pharm ...
written 8 weeks ago by karthic100

Latest awards to karthic

Popular Question 12 weeks ago, created a question with more than 1,000 views. For Genome size estimation using jellyfish
Popular Question 3 months ago, created a question with more than 1,000 views. For Any methods available to do QC analysis of Pacbio raw data??
Scholar 3 months ago, created an answer that has been accepted. For A: perl script for discarding sequences less than 200 nucleotides before running C
Teacher 3 months ago, created an answer with at least 3 up-votes. For A: perl script for discarding sequences less than 200 nucleotides before running C
Popular Question 3 months ago, created a question with more than 1,000 views. For Any methods available to do QC analysis of Pacbio raw data??

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