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UPGMA computation

The unweighted pair group method with arithmetic mean (UPGMA) is a hierarchical clustering method, for example used in phylogeny. In a phylogenetic tree it would result in a global molecular clock ...
xxxcompbioxxx's user avatar
5 votes
0 answers
270 views

convert supplementary reads to primary in sam or bam

I have a problem with a tool, that possibly ignores supplementary reads. I want to find out a bit how this tool works by converting all supplementary reads to primary reads, and then change the names ...
Fini's user avatar
  • 153
5 votes
0 answers
223 views

R Biostrings pairwiseAlignment to BAM

The R package Biostrings has a function to create a pairwiseAlignment from pattern and subject sequences. So far I can save the result into a text file using writePairwiseAlignments. I would like to ...
Green's user avatar
  • 151
5 votes
1 answer
2k views

How to install DnaSP on a Mac

I need to install DnaSp, a nice GUI originally written for Windows for the population genetics of nucleotide sequence data. However, its not working on my mac. I'm using wine to install it using these ...
Mollie Passacantando's user avatar
4 votes
1 answer
85 views

Waterman-Smith-Beyer implementation in Python

I am working on a text aligner to help me get a better understanding of specific steps necessary to perform sequence alignment. So far, things have been going great but I noticed yesterday that my ...
dawnandrew100's user avatar
4 votes
1 answer
37 views

Transposable elements in phylogenetics

I'm very new to phylogenetics and want to build a cladogram from mammal species using pseudogene fragments. The procedure is as follows: Find several query sequences from Gallus gallus of the genes ...
Opossum312's user avatar
4 votes
0 answers
257 views

How to get phylogenetic tree from multiple genes?

I constructed a phylogenetic tree using a gene (example - secA). I had to gather the same gene sequence for all the required species from public database-NCBI and then constructed the tree after ...
abelfit's user avatar
  • 73
4 votes
0 answers
1k views

Kraken2 > OTU format > Phyloseq

A collaborator has passed me over Kraken2 outputs *.report and *.kraken, from a metatranscriptomic sequencing experiment conducted on the minION. I would like to make a tree if the data using a ...
Reebola95's user avatar
3 votes
0 answers
28 views

Add or Simulate Noise in Short-Read Paired End Data

For a project I'm working on, I need to figure out how to model noise that may be happening in real genomes due to alignment errors, contamination, etc. Specifically, short-read paired-end data either ...
user avatar
3 votes
0 answers
718 views

Aligning PacBio HiFi reads to reference genome using pbmm2

I am trying to align a yeast strain sequenced by PacBio HiFi reads to the reference genome S288C (https://www.ncbi.nlm.nih.gov/data-hub/genome/GCF_000146045.2/) using pbmm2 but for some reason I am ...
rimo's user avatar
  • 1,063
3 votes
0 answers
125 views

PSSM Matrix in PSI-BLAST

After running PSI-BLAST one obtains a profile matrix with this header: A R N D C Q E G H I L K M F P S T W Y V How does PSI-...
Caterina's user avatar
  • 307
3 votes
2 answers
555 views

Can't load files into PopART

I am trying to create haplotype networks in PopART (Population genetics with Reticulated Trees*) which I have successfully done many times in the past. Two weeks ago the program was working fine for ...
Gabriella Berman's user avatar
3 votes
0 answers
73 views

How are the values of prop.part() and prop.clades() calculated?

Consider the following dataset: ...
Namenlos's user avatar
  • 317
3 votes
0 answers
61 views

Trying to show the gaps of each seq on bio::Graphics after converting clustalw

I want a box representing each sequence, positioned as they are in the alignment and with gaps shown as breaks in the each box. I've been having trouble for a while with this and have been trying to ...
Jeffery Rosario's user avatar
2 votes
1 answer
31 views

How to adjust QIIME DADA2 parameters to avoid eliminating real sequences

I am working with sequence reads (acquired through MiSeq platform by Illumina) from a viral inoculum. I have already used FastP to merge paired-end reads and cut 5' and 3' ends to remove adapters and ...
forlo_ov_hell's user avatar
2 votes
0 answers
21 views

Understanding the Impact of Parameter Adjustment in KMA Aligner for Gene Analysis

I am currently using the KMA aligner (k-mer alignment) from Clausen et al. (https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-018-2336-6) to analyze gene sequences (metagenomics) and ...
dim's user avatar
  • 155
2 votes
0 answers
45 views

How to create a dataset of contact maps of homologous proteins?

Disclaimer: I am a machine learning researcher working on network science and want to use proteins to test an algorithm of mine using real-world data. My bioinformatics knowledge is minimal. I need to ...
Tendero's user avatar
  • 121
2 votes
1 answer
55 views

Salmon Multiple File SCRIPT giving error

Hi I am using Salmon quantitation for multiple fastq paired files using following code ...
S_Malik's user avatar
  • 61
2 votes
0 answers
280 views

Fst calculation from VCF files

I have four vcf files, SNPs_s1.vcf, SNPs_s2.vcf, SNPs_s3.vcf, and ...
hina's user avatar
  • 21
2 votes
1 answer
64 views

Error importing Maximum Credibility Tree from BEAST into R using treeio's read.beast()

I've encountered an issue that I'm hoping someone can help with. I constructed a phylogenetic tree using BEAST1 and then extracted the Maximum Credibility Tree using treeannotator. I'm trying to ...
Gerald Vasquez Aleman's user avatar
2 votes
0 answers
29 views

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

I am running this command, using the UCSC utilities: bigWigSummary -type=coverage ./galGal6.phastCons77way.bw chr4 25526708 25528708 1 to get phastCons77way ...
VeritatemAmo's user avatar
2 votes
0 answers
133 views

Phylogenetic tree from a large FASTA file

I want to create a phylogenetic tree using a 3.8MB FASTA file with ambiguous code. How can I perform multiple sequence alignment and the construction of phylogenetic tree with these ambiguous codes? ...
user17615's user avatar
2 votes
1 answer
49 views

Parsimony-distance neighborhoods in tree space

I have the following question about the paper A parsimony-based metric for phylogenetic trees by V. Moulton and T. Wu. In this paper, the authors define a "parsimony-distance" between ...
Harry Richman's user avatar
2 votes
0 answers
29 views

Why does segmasker modify headers?

When parsing NCBI BLAST+ segmasker output, I realized the program modifies almost every header containing these strings: ( or )...
maciejwww's user avatar
  • 247
2 votes
1 answer
405 views

How to calculate average BLOSUM62 scores?

I can understand the motive behind the BLOSUM62 matrix, this being a pairwise mutation matrix describing aggregate mutations between the 20 amino acids. However how would you calculate the average ...
dallas_engineer's user avatar
2 votes
0 answers
34 views

Is there a DNAWeaver How-to guide?

Recently I've been trying to use DNA Weaver for customized gene assembly design. Although there is a web version that allows to perform some assembly examples, I've tried to replicate them with python ...
fmjorge99's user avatar
2 votes
0 answers
19 views

Calculate interval of flanking introns

I am looking for a easy way to calculate the intervals of flanking introns based on a transcript annotation file. I have chosen a very complicated method: ...
serbe204's user avatar
2 votes
0 answers
101 views

Bowtie2 gets stuck on alignment

I am aligning a fastq file as follows: ...
justinian482's user avatar
2 votes
0 answers
36 views

Alignment with inserts and keeping the indexing of ref seq intact

Parts of sequences are given below- Reference sequence (pre-alignment): ATTAAAGGTTTATACCTTCCCAGGTAACAAACCAACCAACTTTCGATCTCTTGTAGATCTGTTCTCTAAACGAACTTTAAAATCTGTGT ...
iamakhilverma's user avatar
2 votes
1 answer
116 views

Build tree to calculate beta diversity

I am trying to calculate beta diversity* using the UniFrac distance on my data, each sample having OTUs values. To calculate it, I saw it required building a tree with percentages that represented the ...
odyssey's user avatar
  • 21
2 votes
0 answers
110 views

How to change sequence format in my alignment file?

I have fasta file with alingned several sequences (from MUSCLE), when I open it (e.g. notepad++) they look like: And I want dot format of identities like and then save it in txt file. I failed ...
Adamm's user avatar
  • 216
2 votes
0 answers
368 views

Platanus-allee phasing fail: Error(13): Error, SolveDBG exception!

I am using Platanus-allee 2.2.2 for heterozygous genome (~500mb) assembly with Illumina short reads and PacBio reads input data. I have the file contigs.fa from short reads but phasing step with ...
Enset's user avatar
  • 21
2 votes
0 answers
784 views

Cannot blast against specific NCBI databases

I am having issues with some prokaryote reference genome databases (exact names : ref_prok_rep_genomes.*), that I downloaded from the NCBI website : https://ftp.ncbi.nlm.nih.gov/blast/db/. Files in ...
Olivier Coen's user avatar
2 votes
1 answer
317 views

Read alignment using Bowtie2

So this is related to CRISPR-CAS9. I am working with off-target predictions for my thesis and was looking at all scientific papers related to CRISPR. I found one and decided to use their datasets. The ...
Ina's user avatar
  • 21
2 votes
0 answers
234 views

How snippy makes MSA-like aligned fasta output from multiple samples?

From the log file it seems snippy doesn't do assembly. It only does mapping: fastq --> SAM --> BAM --> VCF --> consensus_seq/snps But if multiple ...
Ahmed Abdullah's user avatar
2 votes
0 answers
325 views

How to get bootstrap support of phylogenetic tree?

I have used multiple sequences aligned file of protein data to generate a maximum parsimony tree, then I used the "bootstrap_trees(msa, times, tree_constructor)" ...
Sidra Younas's user avatar
2 votes
0 answers
49 views

Does anyone have older versions of NT and 16s RNA DB from NCBI?

I am in search of past years' versions of NT and 16s databases from NCBI. I recently contacted NCBI about this and they replied: Unfortunately, we do not archive past versions of the blast ...
ljs's user avatar
  • 265
2 votes
0 answers
211 views

Reproducing population structure from 1000 Genomes Data

I recently tried to reproduce population structure with 1000 Genomes Project data (Phase 3, 2504 people). According to supplementary material, To reduce the dataset, we used VCFtools to only keep ...
In-Hee Lee's user avatar
2 votes
0 answers
32 views

Alignment using secondary and tertiary features of DNA

I m trying to align different sequences of length not greater than 50 bp. Could I incorporate additional information such as stacking energy, entropy, bonds etc as additional criteria in the alignment?...
Aryan Neupane's user avatar
2 votes
1 answer
260 views

Merging ssu-align alignments

ssu-align is an HMM-based MSA tool for ribosome's small subunit (SSU) sequences. It's bundled with three SSU models: archaeal, bacterial eukaryotic Approach Given a set of archaeal and ...
Eli Korvigo's user avatar
1 vote
0 answers
19 views

Metabolite function from DNA sequences

I have an aligned metagenome fasta file. I want to see the relation between the aligned genes and the so-called Clusters of Orthologous Groups (COGs). For the purpose of the analysis I am using the ...
Ivan Ugrin's user avatar
1 vote
1 answer
21 views

How to identify a bacterium species from its short RNA-seq transcriptomics data?

I am new to RNA-seq analysis and wanted to ask if there is a method to reliably identify the species of a microbial organism using only its raw short RNA transcriptomics data. Here are some of the ...
Eshaan IITM's user avatar
1 vote
0 answers
29 views

Guidance Required on Prioritizing Columns for Gene Expression Analysis Using KMA Tool

I am currently in the process of comparing two distinct sets of genes that have been sequenced under two different conditions. My objective is to ascertain whether the expression of specific genes in ...
dim's user avatar
  • 155
1 vote
0 answers
40 views

Problems with pbmm2 alignment after subsampling

I have tested pbmm2 align on my total set of reads. However, the alignments are poor. Therefore I am trying to optimize the parameters with a few of them. After doing a subsampling with samtools -s 0,...
María José's user avatar
1 vote
0 answers
30 views

Large skip after aligning using Cellranger

I have a read from BAM file as following ...
Tien's user avatar
  • 53
1 vote
0 answers
37 views

How to compare CDS, CNE, miRNA, UCNE across new related genomes?

I have 5 sets of raw Illumina whole genome shotgun data from 5 different species, and 3 reference genomes that are assembled/annotated, I want to produce a similar table to Table S2 of this paper: ...
JohnDoe23's user avatar
  • 101
1 vote
1 answer
58 views

Arbovirus phylogenetic analysis using the BEAST2 software via a global clock model

How do I perform a global clock phylogenetic analysis of an arbovirus using the BEAST2 software. If I intend to utilize the global clock model for analysis, kindly guide how to set the parameters of ...
Peter TSAI's user avatar
1 vote
0 answers
25 views

Biopython PhyloTree to PyVis Network

We are trying to convert a Phylogenetic tree to networkx previously calculated with ...
El Dude's user avatar
  • 195
1 vote
0 answers
55 views

java.lang.ArrayIndexOutOfBoundsException: Index 86 out of bounds for length 86

I use the next versions: gatk 4.4.0.0 minimap2 2.26-r1175 samtools 1.19 I have a fastq file. And try to implement gatk MergeBamAlignment to generate a new ...
Shwarz's user avatar
  • 41
1 vote
1 answer
143 views

How to remove third codon positions from a charset in iqtree?

I need to build a phylogenetic tree using IQ-TREE, starting from a sequence alignment in CODON format of several invertebrate mitochondrial genes. These are my charsets: ...
Francesco De Giglio's user avatar