Pub Date : 2025-10-10eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.25012.1
Kerstin Howe, Zoltan Varga, John Postlethwait, Shane A McCarthy, Jonathan M D Wood, Michelle Smith, Karen Oliver
We present the genome assemblies of three females of the Danio rerio strains, AB, Nadia and Cooch Behar (zebrafish; Chordata; Actinopteri; Cypriniformes; Cyprinidae). These assemblies were released in 2020 as part of the Danioninae Sequencing Project. The genome sequence of the strain AB is 1,405.10 megabases, the Nadia strain 1,465.10, and the Cooch Behar strain 1,421.80 megabases in length. Most of the assembly is scaffolded into 25 chromosomal pseudomolecules in each case. For each strain, the mitochondrial genome was also assembled and is 16.6 kilobases in length.
{"title":"The chromosome-level genome sequences of <i>Danio rerio</i> strains AB, Nadia and Cooch Behar.","authors":"Kerstin Howe, Zoltan Varga, John Postlethwait, Shane A McCarthy, Jonathan M D Wood, Michelle Smith, Karen Oliver","doi":"10.12688/wellcomeopenres.25012.1","DOIUrl":"10.12688/wellcomeopenres.25012.1","url":null,"abstract":"<p><p>We present the genome assemblies of three females of the <i>Danio rerio</i> strains, AB, Nadia and Cooch Behar (zebrafish; Chordata; Actinopteri; Cypriniformes; Cyprinidae). These assemblies were released in 2020 as part of the Danioninae Sequencing Project. The genome sequence of the strain AB is 1,405.10 megabases, the Nadia strain 1,465.10, and the Cooch Behar strain 1,421.80 megabases in length. Most of the assembly is scaffolded into 25 chromosomal pseudomolecules in each case. For each strain, the mitochondrial genome was also assembled and is 16.6 kilobases in length.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"559"},"PeriodicalIF":0.0,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12756601/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145901127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-10eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.24968.1
Ian Barnes, Chris Fletcher, Inez Januszczak, Gavin R Broad, Liam M Crowley
We present a genome assembly from an individual male Sussaba pulchella (ichneumonid wasp; Arthropoda; Insecta; Hymenoptera; Ichneumonidae). The genome sequence has a total length of 299.91 megabases. Most of the assembly (81.88%) is scaffolded into 15 chromosomal pseudomolecules. The mitochondrial genome has also been assembled, with a length of 34.69 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.
{"title":"The genome sequence of the ichneumonid wasp, <i>Sussaba pulchella</i> (Holmgren, 1858) (Hymenoptera: Ichneumonidae).","authors":"Ian Barnes, Chris Fletcher, Inez Januszczak, Gavin R Broad, Liam M Crowley","doi":"10.12688/wellcomeopenres.24968.1","DOIUrl":"10.12688/wellcomeopenres.24968.1","url":null,"abstract":"<p><p>We present a genome assembly from an individual male <i>Sussaba pulchella</i> (ichneumonid wasp; Arthropoda; Insecta; Hymenoptera; Ichneumonidae). The genome sequence has a total length of 299.91 megabases. Most of the assembly (81.88%) is scaffolded into 15 chromosomal pseudomolecules. The mitochondrial genome has also been assembled, with a length of 34.69 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"564"},"PeriodicalIF":0.0,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12627938/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145565323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-10eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.24961.1
Emma Sherlock, Keiron D Brown, Chris Fletcher
We present a genome assembly from an individual Bimastos rubidus (Cockspur worm; Annelida; Clitellata; Crassiclitellata; Lumbricidae). The genome sequence has a total length of 812.74 megabases. Most of the assembly (95.63%) is scaffolded into 17 chromosomal pseudomolecules. The mitochondrial genome has also been assembled, with a length of 16.57 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.
{"title":"The genome sequence of the Cockspur worm, <i>Bimastos rubidus</i> (Savigny, 1826) (Crassiclitellata: Lumbricidae).","authors":"Emma Sherlock, Keiron D Brown, Chris Fletcher","doi":"10.12688/wellcomeopenres.24961.1","DOIUrl":"10.12688/wellcomeopenres.24961.1","url":null,"abstract":"<p><p>We present a genome assembly from an individual <i>Bimastos rubidus</i> (Cockspur worm; Annelida; Clitellata; Crassiclitellata; Lumbricidae). The genome sequence has a total length of 812.74 megabases. Most of the assembly (95.63%) is scaffolded into 17 chromosomal pseudomolecules. The mitochondrial genome has also been assembled, with a length of 16.57 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"563"},"PeriodicalIF":0.0,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12576315/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145432234","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-10eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.25028.1
Kerstin Howe, Braedan McCluskey, Zoltan Varga, Bill Trevarrow, Shane A McCarthy, Sarah Pelan, Jonathan M D Wood, Michelle Smith, Karen Oliver
We present a genome assembly from a female specimen of Danio aesculapii (the Panther Danio; Chordata; Actinopteri; Cypriniformes; Cyprinidae). The genome sequence is 1,381.5 megabases in span. Most of the assembly is scaffolded into 25 chromosomal pseudomolecules. Gene annotation of this assembly on Ensembl identified 23,884 protein coding genes.
{"title":"The genome sequence of the Panther Danio, <i>Danio aesculapii</i> Kullander & Fang, 2009.","authors":"Kerstin Howe, Braedan McCluskey, Zoltan Varga, Bill Trevarrow, Shane A McCarthy, Sarah Pelan, Jonathan M D Wood, Michelle Smith, Karen Oliver","doi":"10.12688/wellcomeopenres.25028.1","DOIUrl":"10.12688/wellcomeopenres.25028.1","url":null,"abstract":"<p><p>We present a genome assembly from a female specimen of <i>Danio aesculapii</i> (the Panther Danio; Chordata; Actinopteri; Cypriniformes; Cyprinidae). The genome sequence is 1,381.5 megabases in span. Most of the assembly is scaffolded into 25 chromosomal pseudomolecules. Gene annotation of this assembly on Ensembl identified 23,884 protein coding genes.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"560"},"PeriodicalIF":0.0,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12669980/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145669204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-06eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.24977.1
Liam M Crowley
We present a genome assembly from an individual male Cnephasia stephensiana (Grey Tortrix; Arthropoda; Insecta; Lepidoptera; Tortricidae). The assembly contains two haplotypes with total lengths of 465.14 megabases and 465.69 megabases. Most of haplotype 1 (99.5%) is scaffolded into 30 chromosomal pseudomolecules, including the Z sex chromosome. Haplotype 2 was assembled to scaffold level. The mitochondrial genome has also been assembled, with a length of 16.63 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.
{"title":"The genome sequence of the Grey Tortrix moth, <i>Cnephasia stephensiana</i> (Doubleday, 1850) (Lepidoptera: Tortricidae).","authors":"Liam M Crowley","doi":"10.12688/wellcomeopenres.24977.1","DOIUrl":"10.12688/wellcomeopenres.24977.1","url":null,"abstract":"<p><p>We present a genome assembly from an individual male <i>Cnephasia stephensiana</i> (Grey Tortrix; Arthropoda; Insecta; Lepidoptera; Tortricidae). The assembly contains two haplotypes with total lengths of 465.14 megabases and 465.69 megabases. Most of haplotype 1 (99.5%) is scaffolded into 30 chromosomal pseudomolecules, including the Z sex chromosome. Haplotype 2 was assembled to scaffold level. The mitochondrial genome has also been assembled, with a length of 16.63 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"547"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12775664/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145935123","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-06eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.24183.2
John Mwita Morobe, Samuel Odoyo, Arnold W Lambisia, Edidah Moraa, Charlotte J Houldcroft, Edward C Holmes, George Githinji, Charles N Agoti
In January 2024, the Kenya Ministry of Health issued an outbreak alert following a surge in acute hemorrhagic conjunctivitis (AHC) cases along the Kenyan coast. Our investigations identified coxsackievirus A24 variant (CV-A24v) as the causative agent. In this study, we developed a novel whole genome sequencing assay for CV-A24v, and used it to recover three near complete genomes from the 2024 AHC outbreak in Kenya. This method will support future studies on CV-A24v genomic epidemiology and evolution across Kenya and beyond.
{"title":"Coxsackievirus A24 variant whole genome sequencing from clinical samples using a three overlapping amplicons strategy.","authors":"John Mwita Morobe, Samuel Odoyo, Arnold W Lambisia, Edidah Moraa, Charlotte J Houldcroft, Edward C Holmes, George Githinji, Charles N Agoti","doi":"10.12688/wellcomeopenres.24183.2","DOIUrl":"10.12688/wellcomeopenres.24183.2","url":null,"abstract":"<p><p>In January 2024, the Kenya Ministry of Health issued an outbreak alert following a surge in acute hemorrhagic conjunctivitis (AHC) cases along the Kenyan coast. Our investigations identified coxsackievirus A24 variant (CV-A24v) as the causative agent. In this study, we developed a novel whole genome sequencing assay for CV-A24v, and used it to recover three near complete genomes from the 2024 AHC outbreak in Kenya. This method will support future studies on CV-A24v genomic epidemiology and evolution across Kenya and beyond.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"316"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12569506/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-06eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.24927.1
Lucy Broad, Gavin R Broad
We present a genome assembly from an individual male Netelia melanura (ichneumonid wasp; Arthropoda; Insecta; Hymenoptera; Ichneumonidae). The genome sequence has a total length of 253.87 megabases. Most of the assembly (94.81%) is scaffolded into 7 chromosomal pseudomolecules. The mitochondrial genome has also been assembled, with a length of 28.04 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.
{"title":"The genome sequence of an ichneumonid wasp, <i>Netelia melanura</i> (Thomson, 1888) (Hymenoptera: Ichneumonidae).","authors":"Lucy Broad, Gavin R Broad","doi":"10.12688/wellcomeopenres.24927.1","DOIUrl":"10.12688/wellcomeopenres.24927.1","url":null,"abstract":"<p><p>We present a genome assembly from an individual male <i>Netelia melanura</i> (ichneumonid wasp; Arthropoda; Insecta; Hymenoptera; Ichneumonidae). The genome sequence has a total length of 253.87 megabases. Most of the assembly (94.81%) is scaffolded into 7 chromosomal pseudomolecules. The mitochondrial genome has also been assembled, with a length of 28.04 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"556"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12569507/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-06eCollection Date: 2025-01-01DOI: 10.12688/wellcomeopenres.24898.1
Liam M Crowley, Roger Booth, Michael F Geiser
We present a genome assembly from an individual female Dromius quadrimaculatus (ground beetle; Arthropoda; Insecta; Coleoptera; Carabidae). The genome sequence has a total length of 778.78 megabases. Most of the assembly (95.73%) is scaffolded into 14 chromosomal pseudomolecules, including the X sex chromosome. The mitochondrial genome has also been assembled, with a length of 16.57 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.
{"title":"The genome sequence of a ground beetle, <i>Dromius quadrimaculatus</i> (Linnaeus, 1758) (Coleoptera: Carabidae).","authors":"Liam M Crowley, Roger Booth, Michael F Geiser","doi":"10.12688/wellcomeopenres.24898.1","DOIUrl":"10.12688/wellcomeopenres.24898.1","url":null,"abstract":"<p><p>We present a genome assembly from an individual female <i>Dromius quadrimaculatus</i> (ground beetle; Arthropoda; Insecta; Coleoptera; Carabidae). The genome sequence has a total length of 778.78 megabases. Most of the assembly (95.73%) is scaffolded into 14 chromosomal pseudomolecules, including the X sex chromosome. The mitochondrial genome has also been assembled, with a length of 16.57 kilobases. This assembly was generated as part of the Darwin Tree of Life project, which produces reference genomes for eukaryotic species found in Britain and Ireland.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"10 ","pages":"555"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12759285/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145901087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-06eCollection Date: 2023-01-01DOI: 10.12688/wellcomeopenres.20012.2
Janna Hastings, Martin Glauer, Robert West, Anna Kleinau, James Thomas, Alison J Wright, Susan Michie
Background: Systematic reviews of effectiveness estimate the relative average effects of interventions and comparators in a set of existing studies e.g., using rate ratios. However, policymakers, planners and practitioners require predictions about outcomes in novel scenarios where aspects of the interventions, populations or settings may differ. This study aimed to develop and evaluate an ontology-informed, interpretable machine learning algorithm to predict smoking cessation outcomes using detailed information about interventions, their contexts and evaluation study methods. This is the second of two linked papers on the use of machine learning in the Human Behaviour-Change Project.
Methods: The study used a corpus of 405 reports of randomised trials of smoking cessation interventions from the Cochrane Library database. These were annotated using the Behaviour Change Intervention Ontology to classify, for each of 971 study arms, 82 features representing details of intervention content and delivery, population, setting, outcome, and study methodology. The annotated data was used to train a novel machine learning algorithm based on a set of interpretable rules organised according to the ontology. The algorithm was evaluated for predictive accuracy by performance in five-fold 80:20 cross-validation, and compared with other approaches.
Results: The machine learning algorithm produced a mean absolute error in prediction percentage cessation rates of 9.15% in cross-validation, which was lower than the mean absolute error of other approaches including an uninterpretable 'black-box' deep neural network (9.42%), a linear regression model (10.55%) and a decision tree-based approach (9.53%). The rules generated by the algorithm were synthesised into a consensus rule set to create a publicly available predictive tool to provide outcome predictions and explanations in the form of rules expressed in terms of predictive features and their combinations.
Conclusions: An ontologically-informed, interpretable machine learning algorithm, using information about intervention scenarios from reports of smoking cessation trials, can predict outcomes in new smoking cessation intervention scenarios with moderate accuracy.
{"title":"Predicting outcomes of smoking cessation interventions in novel scenarios using ontology-informed, interpretable machine learning.","authors":"Janna Hastings, Martin Glauer, Robert West, Anna Kleinau, James Thomas, Alison J Wright, Susan Michie","doi":"10.12688/wellcomeopenres.20012.2","DOIUrl":"10.12688/wellcomeopenres.20012.2","url":null,"abstract":"<p><strong>Background: </strong>Systematic reviews of effectiveness estimate the relative average effects of interventions and comparators in a set of existing studies <i>e.g.,</i> using rate ratios. However, policymakers, planners and practitioners require predictions about outcomes in novel scenarios where aspects of the interventions, populations or settings may differ. This study aimed to develop and evaluate an ontology-informed, interpretable machine learning algorithm to predict smoking cessation outcomes using detailed information about interventions, their contexts and evaluation study methods. This is the second of two linked papers on the use of machine learning in the Human Behaviour-Change Project.</p><p><strong>Methods: </strong>The study used a corpus of 405 reports of randomised trials of smoking cessation interventions from the Cochrane Library database. These were annotated using the Behaviour Change Intervention Ontology to classify, for each of 971 study arms, 82 features representing details of intervention content and delivery, population, setting, outcome, and study methodology. The annotated data was used to train a novel machine learning algorithm based on a set of interpretable rules organised according to the ontology. The algorithm was evaluated for predictive accuracy by performance in five-fold 80:20 cross-validation, and compared with other approaches.</p><p><strong>Results: </strong>The machine learning algorithm produced a mean absolute error in prediction percentage cessation rates of 9.15% in cross-validation, which was lower than the mean absolute error of other approaches including an uninterpretable 'black-box' deep neural network (9.42%), a linear regression model (10.55%) and a decision tree-based approach (9.53%). The rules generated by the algorithm were synthesised into a consensus rule set to create a publicly available predictive tool to provide outcome predictions and explanations in the form of rules expressed in terms of predictive features and their combinations.</p><p><strong>Conclusions: </strong>An ontologically-informed, interpretable machine learning algorithm, using information about intervention scenarios from reports of smoking cessation trials, can predict outcomes in new smoking cessation intervention scenarios with moderate accuracy.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"8 ","pages":"503"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12603517/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145507446","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-06eCollection Date: 2024-01-01DOI: 10.12688/wellcomeopenres.21224.2
Denise C Wawman
We present a genome assembly from an individual male Pasiphila rectangulata (the Green Pug; Arthropoda; Insecta; Lepidoptera; Geometridae). The genome sequence is 582.5 megabases in span. Most of the assembly is scaffolded into 30 chromosomal pseudomolecules, including the Z sex chromosome. The mitochondrial genome has also been assembled and is 15.74 kilobases in length. Gene annotation of this assembly on Ensembl identified 17,153 protein coding genes.
{"title":"The genome sequence of the Green Pug moth, <i>Pasiphila rectangulata</i> (Linnaeus, 1758).","authors":"Denise C Wawman","doi":"10.12688/wellcomeopenres.21224.2","DOIUrl":"10.12688/wellcomeopenres.21224.2","url":null,"abstract":"<p><p>We present a genome assembly from an individual male <i>Pasiphila rectangulata</i> (the Green Pug; Arthropoda; Insecta; Lepidoptera; Geometridae). The genome sequence is 582.5 megabases in span. Most of the assembly is scaffolded into 30 chromosomal pseudomolecules, including the Z sex chromosome. The mitochondrial genome has also been assembled and is 15.74 kilobases in length. Gene annotation of this assembly on Ensembl identified 17,153 protein coding genes.</p>","PeriodicalId":23677,"journal":{"name":"Wellcome Open Research","volume":"9 ","pages":"256"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12569505/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}