How to select homologous sequences from BLAST search to generate multiple sequence alignment?
I mean how many sequences, what is the best E-value cut-off for these sequences.
One could generate an MSA for a short stretch of AA's that includes a domain (or some other converved sequence) or you may be referring to a full length protein.
I performed blast searches (with an e-value cut-off of 1E-5) on de novo assembled transcripts against the ncbi nr database. Many transcripts received hits with …
Hello guys, I have more than 10,000 de novo assembled unigenes from RNA-seq, and blasted them against 95 protein sequences from another insect species get …
<p>Hi Friends,</p> <p>After doing blast for my nucleotide sequence i have found out the homologous sequence based on the identity, sequence coverage and e value. …
<p>Hello.</p> <p>I am using mutliple alignments for some years and I always use the same protocol:</p> <ol> <li>I search homologous sequences in a database </li> …
There isn't a fixed value for this. Take a look at: http://biology.stackexchange.com/questions/19338/e-value-blast-cut-off
One could generate an MSA for a short stretch of AA's that includes a domain (or some other converved sequence) or you may be referring to a full length protein.
Thank you for you response, OK so If I want to identify conserved regions I should go with smaller E-value right?
In general, yes. But keep the caveats defined in the stackexchange post in mind as you go about doing this.