ArticleBio-protocol2020
High-resolution and Deep Phylogenetic Reconstruction of Ancestral States from Large Transcriptomic Data Sets.
Article in Bio-protocol, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed, 5 citations in OpenAlex.
- A genomic toolkit for winged bean Psophocarpus tetragonolobus.Nature communications · 2024Article
- Pole position: How plant cells polarize along the axes.The Plant cell · 2022Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phylogenetics is an important area of evolutionary biology that helps to understand the origin and divergence of genes, genomes and species. Building meaningful phylogenetic trees is needed for the accurate reconstruction of the past. To achieve a correct phylogenetic understanding of genes or proteins, reliable and robust methods are needed to construct meaningful trees. With the rapidly increasing availability of genome and transcriptome sequencing data, there is a need for efficient and accurate methodologies for ancestral state reconstruction. Currently available methods are mostly specific for certain gene families, and require substantial adaptation for their application to other gene families. Hence, a generalized framework is essential to utilize large transcriptome resources such as OneKP and MMETSP. Here, we have developed a flexible yet efficient method, based on core strengths such as emphasis on being inclusive in homolog selection, and defining orthologs based on multi-layered inferences. We illustrate how specific steps can be modified to fit the needs of any protein family under consideration. We also demonstrate the success of this protocol by studying and testing the orthologs in various gene families. Taken together, we present a protocol for reconstructing the ancestral states of various domains and proteins across multiple kingdoms of eukaryotes, using thousands of transcriptomes.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.