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Maximilian Press's user avatar
Maximilian Press's user avatar
Maximilian Press
  • Member for 6 years, 3 months
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1 vote
Accepted

What's the difference between Barycenter Centrality and Closeness Centrality (Freeman)?

1 vote

List of global ethnicities

1 vote

Determine if an organism is microbic or unicellular

1 vote

How to modify DNA evolution model to fit actual data?

1 vote

Gap-fill assembly with PacBio reads

1 vote

Display a score or graph to visualize the degree of conservation of each residue from alignment data

1 vote

repophlan script to download bacterial genome

1 vote

pvalue calculation of protein-protein network with permutation test

1 vote

hgsql not found when running a script despite being accessible on command-line

1 vote

How do I get the adjacency matrix from gene similarity network?

1 vote
Accepted

HVG and variation coefficient

1 vote

Replicate papers (beginner)

1 vote

Make a fasta out of mapped reads without taking into account the reference

1 vote

Random networks in PPi

1 vote

Optimum parameters for genome assembly via canu

1 vote

polishing assembled genome to QV50 value

1 vote

Cuffmerge: EOF marker is absent. The input is probably truncated

1 vote

Is there any value in scaffolding the output contigs of MEGAHIT assembler given a metagenomic dataset?

1 vote

Phylogenetics analysis between diverse species

1 vote

Why do we scale the rate matrix of a substitution model to make the average rate of substitution equal 1?

1 vote

Visualizing cell growth

1 vote
Accepted

Scooping and GeneMatcher

1 vote
Accepted

How to fix NameError?

1 vote
Accepted

Metagenomics: Identifying most common sequences

1 vote

Add tags to the read pairs in a bam file

1 vote

biopython-motifs , How can I create motif from sequences of different length?

1 vote
Accepted

Multiple Alignment cost application

1 vote
Accepted

How to calculate RNA copies in qPCR using R?

1 vote
Accepted

Is it possible to filter contaminated reads for raw PacBio sequences (not HiFi reads) before assembly?

1 vote

genotyping or variant calling in R