ArticleScientific data2025
Chromosome-level genome assembly of the short-faced mole (Scaptochirus moschatus).
Article in Scientific data, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
The short-faced mole (Scaptochirus moschatus) belonging to the family Talpidae in the order Eulipotyphla is a good model for studying adaptive evolution of mammals because of its morphological and ecological characteristics. However, the lack of genome of short-faced mole has hindered previous studies. In this study, we assembled the genome of the short-faced mole based on Illumina, PacBio HiFi and Hi-C sequencing, and acquired the genome of the short-faced mole with the size of 2.17 Gb. 99.6% of the assembled genome were identified as complete BUSCOs, including 90.7% as complete single-copy BUSCOs and 8.9% as complete duplicated BUSCOs. The assembled genome was anchored to 24 chromosomes with an anchor rate of 94.33%, of which the 24th chromosome (Chr 24) probably contained the X and Y chromosomes. A total of 21,139 coding genes were predicted, and 8.58 exons per gene were predicted.
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.