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3 votes
2 answers
67 views

efetch multiple records at once

0 votes
1 answer
80 views

How to pack up a Python script in the form a Dockerfile

3 votes
2 answers
60 views

Remote NCBI's Blast Perl API: maximising hits returned via command line

1 vote
1 answer
34 views

Do we design primers for single stranded DNA with same criteria as we do for double stranded DNA?

2 votes
1 answer
56 views

Trimmomatic QC report shows drop in the reads and presence of overrepresented sequences

1 vote
1 answer
57 views

Using average of sequence similarities when delimiting genera - how to deal with outliers?

0 votes
1 answer
30 views

How to find amino acid sequence of a given protein

0 votes
0 answers
34 views

Would DESeq2 be appropriate or should I use another tool for differential gene expression?

0 votes
1 answer
27 views

Mapping List of Probes/Primers/Short Oligos to a Reference Fasta/q

2 votes
1 answer
21 views

Is a classification tree appropriate method to use for my project?

4 votes
0 answers
24 views

Linking GenBank records to biosamples (and vice versa) using edirect

-1 votes
0 answers
23 views

Phred score calculation

-1 votes
0 answers
21 views

Source to learn processing of Sequencing data [closed]

0 votes
0 answers
19 views

how is log2foldchange calculated in DESeq2

0 votes
0 answers
18 views

Is there a method/web server to generate Position-specific scoring matrix (PSSM) for nucleotide sequences (DNA/RNA)?

2 votes
0 answers
15 views

How come bigWigSummary shows coverage greater than 1 for some region of the genome?


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