Questions tagged [phylogenetics]

Phylogenetics is the study of evolutionary relationships among biological entities - often species, individuals or genes.

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How can I get data of single cell RNA sequence with raw count?

I am using dataset GSE85241, but I can't find the read counts of the dataset. It only provides with RPKM values. How can I find the read counts of a dataset?
Kevis Lin's user avatar
1 vote
0 answers
20 views

Calculating the effect of differences between two groups of nucleotide sequences at every position

I'm investigating two different groups of short nucleotide sequences. The behaviour of a certain DNA-binding protein is likely influenced by common differences between these two groups leading high or ...
beginbio's user avatar
2 votes
2 answers
62 views

How can I improve or otherwise investigate an unreliable genome tree?

Summary My genome tree doesn't agree with my gene trees and I get the feeling that my genome tree might be wrong, possibly due to long branch attraction, but I don't know how to check/fix it. ...
Laura's user avatar
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1 vote
2 answers
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Generate consensus protein sequence from relatively gappy alignment?

I would like to know what would be the best way to generate a full-length consensus sequence? I want to obtain a single representative sequence from a relatively gappy multiple sequence alignment of ...
719016's user avatar
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2 votes
1 answer
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ggtree:How to keep leading zero ‘0’ in the tiplabel?

I am using ggtree to draw a phylogenetic tree. Some taxa IDs have a 0 at the beginning. However, when I plot the tiplabel the leading zero is automatically dropped. ...
YP CHEN's user avatar
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0 answers
158 views

Extract SNPs from multiple sequence alignment

I’m wondering if folks have recommendations for tools/scripts to extract SNP sites from a multiple sequence alignment of consensus bacterial genomes? Specifically, I am interested in a multiple ...
ksw's user avatar
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3 votes
1 answer
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What does this accession NCBI code mean: 6MWN_B?

According to this article, accession codes should consist from a combination of uppercase letters following a combination of digits. If this is a RefSeq, it can have a prefix as a combination of ...
Vovin's user avatar
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1 vote
2 answers
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Phylogenetic tree building from proGenomes database for shotgun metagenomics

For some weeks I'm fighting with an issue about phylogenetic tree building to use in a phyloseq object in order to calculate beta-diversity metrics that takes into account phylogenetic distance. I’m ...
MagíBC's user avatar
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3 votes
1 answer
52 views

Phylogenetic tree rooting in shotgun metagenomics

But I have some weeks fighting with this issue about phylogenetic tree building to use in a phyloseq object in order to calculate beta-diversity metrics that takes into account tree distance branches ...
MagíBC's user avatar
  • 41
1 vote
1 answer
101 views

Select synonymous sites from a multiple sequence alignment

Could someone kindly recommend a tool or R package that can identify synonymous sites in a multiple sequence alignment? I wish to select those taxa for tree reconstruction and other downstream ...
ksw's user avatar
  • 111
2 votes
1 answer
73 views

Biopython reads my tree eternally long

I have a nexus tree (1332 taxa) with a lot of additional data. When I tried to read it through tree = Phylo.read(treepath, "nexus"), my kernel got ...
Vovin's user avatar
  • 435
3 votes
1 answer
65 views

What is & how to solve File error: my.xml.state (Remote I/O error)?

I caught the next exception during my phylogeographical analysis in BEAST 2 with GEO_SPHERE. What could be the reason? & how to evade this in the future? ...
Vovin's user avatar
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4 votes
1 answer
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Tree Building Algorithm that treats gaps as deletions

I'm part of a nanopore sequencing experiment that will sequence several generations of viruses. The intent is to perform directed evolution by putting selective pressure on these viruses and tracking ...
CCranney's user avatar
3 votes
4 answers
897 views

How can I add a ";" at the end of each fasta header line in a file?

I have a large fasta file with RNA sequences. I need to add a ; at the end of each header line (lines beginning with >) in ...
Callahan McGovern's user avatar
0 votes
0 answers
51 views

What is the best tools to find all the somatic mutations?

I am a beginner in this field. I would like to know which is the best way to get all the mutations from a certain sample. At this point, I am considering using GATK (here) and Maftools (here). I don't ...
Scott XU's user avatar
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4 votes
2 answers
209 views

What can be the reason of getting negative branches lengths after BEAST analysis?

BEAST2 is currently being used for tree reconstruction prior phylogeographic analysis. The sample size and loci are described below. I thought that BEAST/BEAST2 does not allow negative lengths of ...
Vovin's user avatar
  • 435
3 votes
1 answer
102 views

Missing ',' in line when Biopython reads a nexus tree

I want to edit a tree that I got from BEAST2 treeannotator in nexus-format. Usually I use the module Phylo from Biopython for such work but ...
Vovin's user avatar
  • 435
2 votes
1 answer
107 views

Is it possible to reconstruct an MSA with PSSM?

I am thinking of reconstructing an multiple sequence alignment (MSA) of protein sequences from a position-Specific Scoring Matrices (PSSM). Is it possible? I suppose co-evolution information is lost ...
Johnny Tam's user avatar
0 votes
1 answer
298 views

BEAGLE do not see and/or not use OpenCL

I am conducting phylogeny analyses using BEAST 2 as software tool. It is said that it can be accelerated by BEAGLE-library. I have a personal laptop with Windows & a cluster with CentOS. I ...
Vovin's user avatar
  • 435
3 votes
1 answer
357 views

What is the meaning of "Filtering allele frequency" in the gnomAD database?

Recent gnomAD versions include a "filtering allele frequency" which tells you when a variant can be safely adjudged not to be disease-causing. Unfortunately, I'm having trouble making sense ...
Jeff's user avatar
  • 31
1 vote
1 answer
92 views

Convert Arlequin ("DNA" markers) to Genepop (PGDspider or otherwise)

I have Arlequin output files (*.arp) from fastSimcoal2 that I'm trying to convert to genepop files (to read into adegenet). The Arlequin files are using the "DNA" marker (50 bp long), and ...
akoontz11's user avatar
-1 votes
2 answers
48 views

How to use GEO_SPHERE?

I have some problems with geosphere package which extends/applies the Beast Bayesian MCMC package for calculating phylogenetic trees. Please, could anyone give any hints about at least one of them? ...
Vovin's user avatar
  • 435
3 votes
4 answers
367 views

How to programatically download SARS-CoV-2 fasta from NCBI/Genbank via API?

I would like to download a number of SARS-CoV-2 fastas from NCBI/Genbank using a web endpoint. I looked on their website but it's confusing. I have the accession numbers, but can't figure out how to ...
Cornelius Roemer's user avatar
2 votes
1 answer
95 views

Where to get BED files for regions that contain binding site motifs for specific transcription factors?

Quick question, is there a place where one can download BED files for the binding motifs of certain transcription factors. In my case, I'm looking for a BED file for the genomic regions (enhancers) ...
user305902's user avatar
2 votes
1 answer
69 views

Questions about microbial 16s rRNA phylogenetic, ANI Taxonomy, and GGDC

I have a few questions about these three methods. We commonly use 16s rRNA to identify species and construct a phylogenetic tree. If there's a new isolate from a new and undiscovered ecosystem, ...
raysteven's user avatar
4 votes
1 answer
151 views

LD Score Regression Derivation hard to follow

I am trying to understand the derivations from Sullivan et al. (2015) in the Supplementary Material. There, it is mentioned in the first page that the least squares estimate of the j-th SNP effect, ...
Vasilis Lemonidis's user avatar
3 votes
2 answers
778 views

Hirschberg's Alignment Algorithm Implementation. Works on the wiki example but not on large sequences of dissimilar size

I implemented Hirschberg's algorithm in python and used the wiki example to verify correct implementation given the scoring parameters and sequences: ...
user3754317's user avatar
4 votes
1 answer
85 views

Co-occurrence networks in Metagenomics studies

I have recently acquired some 16S metagenomics data, and was wondering if anyone can speak of the potential limitations, challenges as well as advantages to conducting a network-based study on ...
h3ab74's user avatar
  • 836
2 votes
1 answer
35 views

Protein-coding gene evolution age and species divergence time: are they correlated?

Is it possible to infer protein-coding gene evolution age by species divergence time? For example, species A diverged 300 million years (MYA) ago from its common ancestor with species C, whilst ...
Johnny Tam's user avatar
0 votes
1 answer
90 views

How to solve correlation problems between different samples in scRNA-seq?

I am trying to align and merge different samples from NCBI. I end up having correlation problem with these sample. The picture below shows an heatmap of the R² by doing a linear regression between 2 ...
Alexis Finkbeiner's user avatar
1 vote
2 answers
123 views

Bio.codonalign.codonseq module (cal_dn_ds) for SARS-COV-2

I have calculated the dN,dS ratio for a SARS-COV-2 data set ('NC_045512.2' (Wuhan strain) and 'LC666924.1'), and results in a zero value (for most of the genes). Is it possible and what is the ...
Alex's user avatar
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2 votes
1 answer
204 views

No bootstrap value on single-copy gene tree created by OrthoFinder

I'm running analysis with OrthoFinder and it produces a single-copy gene tree. When I visualize the tree with iTOL, there's no bootstrap value on the branches or nodes. There's a published paper in ...
raysteven's user avatar
3 votes
2 answers
131 views

How to get the number of complete phage genomes available on ncbi?

I am looking to establish the total number of complete phage genomes available on NCBI. I am not looking for any specific type, but want to understand the total diversity available. How can I perform ...
pietro_molina's user avatar
2 votes
2 answers
47 views

Is there a publication database or search engine offering geneID or UniProtID correlation?

Do we have a publication database or search engine that offers geneID or UniProtID correlation? For example, I search "IPS cells" -> I want to know what genes or proteins are under active ...
Johnny Tam's user avatar
1 vote
2 answers
45 views

Mapping NCBI taxID to divergence time?

I want to map NCBI taxID, specifically a pair of Genbank sequences, to the divergence time estimate of their common ancestor. For example, using a coalescence theory approach predominantly used in ...
Johnny Tam's user avatar
2 votes
1 answer
27 views

Independent Subset of Rectangles Problem for Nonoverlapping local alignments

I'd like to implement a graph-based algorithm for DNA comparison, more especially by solving a problem that can be formulated as a Maximum Weighted Independent Set problem. I have found the article in ...
user12910's user avatar
  • 121
1 vote
2 answers
419 views

What is the most appropriate way to find the most recent common ancestor between two distantly related species

I want to specifically find the common ancestor between a lobster and a humans. I suspect it was an aquatic worm of some description. But I want to know about the nervous system of this common ...
syn_bio_delta's user avatar
1 vote
2 answers
48 views

Remove variable sequence component within a tree text file

I have a gene tree file of 436 orthologue genes from 6 species. I want to remove unwanted extensions as it looks massy after visualization. My file looks like: (TRINITY_Clupea_DN5452_c0_g1_i1.p1:0....
Kishor Kumar Sarker's user avatar
3 votes
3 answers
243 views

Correspondence of SARS-CoV-2 annotations (Nextstrain clades - Pango lineages)

Is there any annotation file providing correspondence between Nextclade and Pangolin variant nomenclature/annotations, to annotate some SARS-CoV-2 genomes from Gisaid with both these? For the moment I ...
aechchiki's user avatar
  • 2,676
2 votes
1 answer
64 views

At what point is a gene different between species that we call it a different gene?

I am new to genetics and I know humans share many genes with mice for instance but that there are slight differences in conserved nucleotide sequences. Is there a community consensus around at what ...
Angus Campbell's user avatar
0 votes
0 answers
19 views

Generating intercalation site in DNA for custom sequence

Thank you for your help. Can anybody please tell me how I can generate an intercalation site in DNA at the base pairs I am interested on. I appreciate if you can please guide me to any tutorials or ...
dnalectronics's user avatar
0 votes
1 answer
122 views

Help me in understanding the PDB file

Can anybody please explain the below line to me. "We took the structure and coordinates of nogalamycin from the X-ray structure determined in PDB code = 1D17" What do I need to download from ...
dnalectronics's user avatar
1 vote
0 answers
33 views

What exactly is a reasonable evolutionary criterion? [closed]

I got a rejection of publication which the reviewers mainly point out as not following a reasonable evolutionary criterion for choice of species used for phylogeny creation. In our dataset, a list of ...
007's user avatar
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0 votes
0 answers
14 views

xtract from eutilities not exctracting the information I need

I'm running the following command which uses the NCBI e-utilities: esearch -db bioproject -query "PRJNA198476 [PRJA]" | esummary This returns: ...
An Ignorant Wanderer's user avatar
2 votes
1 answer
81 views

Simulation of DNA sequences through substitution rates

I'm looking for a little bit of guidance. My question is regarding the simulation of DNA sequences with a fix substitution rate. The majority of the programs for simulating sequences use Continuous ...
Kako's user avatar
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1 vote
1 answer
64 views

Given SNP-Chip data for a population, what tool should I use to reconstruct haplotypes?

I think Eagle or haploSep will do the job of reconstructing haplotype data, but I'm not sure what the 'standard' or best practice tool to use is. I have a VCF/PLINK format file of ~8,000 individuals ...
Dan Bolser's user avatar
1 vote
2 answers
75 views

Getting translation table of organisms through Entrez direct (or other CLIs)

I have a long list of NCBI taxonomic ids for organisms and I want to write a script to get their corresponding translation tables. Is there a way to do this through Entrez? (packages in R, Python etc. ...
weddegege's user avatar
1 vote
1 answer
72 views

building complex drug-dna for AMBER software

I will appreciate if you can please clarify some of my doubts about drug-DNA complex. I want to study the drug-DNA simulation using AMBER. I did go through all the tutorials video on youtube but ...
dnalectronics's user avatar
0 votes
1 answer
40 views

What to use to determine SNPs in a population? How to find significant SNP variation between generations?

I have a population in the hundreds and did an Illumina pool-seq (ended up with ~100bp reads for the whole population). I have the reference genome for the species and now need to align all the ...
gl00ten's user avatar
  • 249
1 vote
2 answers
249 views

Permutations of 4 amino acid sequence oligopeptide

I have an assignment for a project to build a tetrapeptides library to screen against some target enzymes in silicon. I am looking for a script to construct about 160000 tetrapeptide from the 20Amino ...
Ruthy's user avatar
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