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Fig. 3. Phylogenetic trees from reported 18S in Molecular systematics analysis of Lymantria dispar based on 18S rRNA and cox1 mtDNA sequence data
Fig. 3. Phylogenetic trees from reported 18S rRNA genes of insects according to NJ. A. Based on sequences of full-length. B. Based on second conserved region.
Fig. 4 in Molecular systematics analysis of Lymantria dispar based on 18S rRNA and cox1 mtDNA sequence data
Fig. 4. Phylogenetic trees based on partial sequences from reported cox1 genes of insects according to NJ.
Fig.1 in Molecular systematics analysis of Lymantria dispar based on 18S rRNA and cox1 mtDNA sequence data
Fig.1. PCR result of 18S rRNA of Lymantria dispar. Separated bands (from left to right). 18S1, 18S2, 18S rRNA, DL2000 marker.
Fig. 5. Sequence variation among 4 28S in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California
Fig. 5. Sequence variation among 4 28S genotypes identified from Oligonychus perseae populations in California, Mexico, and Costa Rica. Genotypes are named according to 3 genetic clusters identified from cytochrome oxidase subunit 1 (COI) haplotypes (see Fig. 2).
Fig. 3. Sequence variation among 4 internal transcribed spacer 2 in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California
Fig. 3. Sequence variation among 4 internal transcribed spacer 2 (ITS2) genotypes identified from Oligonychus perseae populations in California,Mexico, and Costa Rica. Genotypes are named according to 3 genetic clusters identified from cytochrome oxidase subunit 1 (COI) haplotypes (see Fig. 2).
Fig. 4 in Marked genetic diversity within Blastocystis in Australian wildlife revealed using a next generation sequencing-phylogenetic approach
Fig. 4. Relative abundance of Blastocystis subtypes (STs) in marsupial and deer species. Marsupials are represented by eastern grey kangaroos and wallabies; deer are represented by red, fallow and sambar deer. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Marked genetic diversity within Blastocystis in Australian wildlife revealed using a next generation sequencing-phylogenetic approach
Fig. 3. Phylogenetic analysis of SSU-rRNA sequence data (aligned over 2035 positions) to infer the relationships of recognised Blastocystis subtypes (STs) as well as new STs discovered in the present study. The tree was constructed using Bayesian Inference method (MrBayes) and used Proteromonas lacertae as an outgroup. Posterior probabilities less than 0.95% are not displayed. The two novel subtypes and additional ST13 and ST24 sequences are indicated in bold. After the present analysis was completed, Santín et al. (2023) reported a subdivision of "ST10" into four STs (i.e. ST10, ST42, ST43 and ST44).
Fig. 2 in Marked genetic diversity within Blastocystis in Australian wildlife revealed using a next generation sequencing-phylogenetic approach
Fig. 2. Diagram of the method used to obtain sequence for a SSU-rRNA gene region (~1750 bp) of Blastocystis. Two primer sets were used to obtain overlapping sequences for this region.
Fig. 7 in Comprehensive Analysis of the Jellyfish (Goette, 1886) (Semaeostomeae: Pelagiidae) with Description of the Complete rDNA Sequence.
Fig. 7. Nucleotide divergences of the cnidarians 18S and 28S rDNAs (datasets used in Table 1) based on corrected p-distances. Genetic distances between each paired sequence were calculated by the Kimura 2-parameter model, where a total of 16 cnidarian species were compared. Statistical analysis showed that the 18S rDNA divergences were significantly different from those of 28S rDNA (Student t-test, P <0.05, N = 66).
Fig. 6 in Comprehensive Analysis of the Jellyfish (Goette, 1886) (Semaeostomeae: Pelagiidae) with Description of the Complete rDNA Sequence.
Fig. 6. Phylogenetic relationships of the family Pelagiidae, including the genera Chrysaora, Pelagia and Sanderia, inferred from 18S rDNA (A), 28S rDNA (B) and morphological characters (C), which were redrawn from Fig. 95 in Morandini and Marques (2010). Phylogenetic trees of the rDNAs were constructed using the maximum-likelihood (ML) algorithms with the GTR+G model. A jellyfish Cyanea capillata (the family Cyaneidae) was used as the outgroup. Additional Bayesian trees generated similar branch patterns. The first and second numbers at the nodes display bootstrap proportions (BP) and posterior probabilities (PP) obtained in the ML and Bayesian analyses, respectively. Branch lengths are proportional to the scale given. Thick lines represent congruent branches between 18S and 28S, and morphological systematics.
Fig. 4. A in Comprehensive Analysis of the Jellyfish (Goette, 1886) (Semaeostomeae: Pelagiidae) with Description of the Complete rDNA Sequence.
Fig. 4. A dot matrix comparison of rDNA sequences between Chrysaora pacifica (KY 212123) and Aurelia coerulea (EU276014). Color scale bars represent consecutive sequence length of some regions detected similarly between the two sequence pairs. The open boxes in matrices indicate rDNA coding regions such as 18S, 5.8S, and 28S.
Fig. 2. A in Comprehensive Analysis of the Jellyfish (Goette, 1886) (Semaeostomeae: Pelagiidae) with Description of the Complete rDNA Sequence.
Fig. 2. A schematic representation of the single unit of rDNA (A), and GC content (%), nucleic acid distribution (% thymine), sequence complexity, and entropy (dS) in 100-bp windows across the entire rDNA nucleotides of Chrysaora pacifica (B). In the full rDNA (A), solid boxes indicate the ribosomal RNA genes and thin lines represent ITS or IGS. Nucleotide sequences in length and GC composition of each locus are represented near a line by calculation from a single unit of rDNA. The putative transcription start site is represented by an arrow; solid inverted-triangles represent sub-repeats in IGS.
Fig. 5. Phylogenetic relationships between jellyfishes within the order Semaeostomeae inferred from nearly complete 18S in Comprehensive Analysis of the Jellyfish (Goette, 1886) (Semaeostomeae: Pelagiidae) with Description of the Complete rDNA Sequence.
Fig. 5. Phylogenetic relationships between jellyfishes within the order Semaeostomeae inferred from nearly complete 18S rDNA (A) and partial 28S rDNA sequences (B) with maximum-likelihood (ML) algorithms. ML analyses of 18S and 28S were used as the nucleotide substitution model of GTR+G. Two hydrozoans (Hydractinia echinata and Podocoryne carnea for 18S rDNA; Astrohydra japonica and Melicertissa sp. for 28S) were included as the outgroups. Additional Bayesian analysis generated similar topology of the tree compared with the ML tree. Posterior probabilities (PP) from the analyses were incorporated into the ML tree to support the strength of each branch. The first and second numbers at the nodes display bootstrap proportions (BP) (> 50%) in ML and PP (> 0.50) in Bayesian, respectively. Branch lengths are proportional to the scale given. *Represents controversial species names, because they were suspected as different species by Bayha et al. (2017).
Fig. 1 in Comprehensive Analysis of the Jellyfish (Goette, 1886) (Semaeostomeae: Pelagiidae) with Description of the Complete rDNA Sequence.
Fig. 1. Live Chrysaora pacifica in natural habitat: basolateral (A and B), lateral (C) and apical view (D).
Nanotiming: single-molecule based, telomere-to-telomere DNA replication timing profiling by nanopore sequencing
<p>Dataset for the manuscript "Nanotiming: telomere-to-telomere DNA replication timing profiling by nanopore sequencing" by Theulot et al ,2024 (<span>https://doi.org/10.1038/s41467-024-55520-3</span>) related to the github repository (https://github.com/LacroixLaurent/NanoTiming)</p> <ul> <li>WT_rep3.tar.gz contains fast5 file from an experiment where yeast BT1 strain was grown for one doubling time with 5µM BrdU then DNA was sequenced on R9.4.1 ONT flowcell</li> <li>mod_mapping.bam contains the bam file resulting from the BrdU base calling with megalodon (v2.2.9) using our BT1 reference genome and our BrdU aware model for base-calling</li> <li>WT_rep3_nanoT.bed.gz contains the reads coordinates from the mod_mappings file</li> <li>WT_rep3_nanoT_alldata.rds contains the BrdU profiles for each reads of the mod_mappings file, with the BrdU signal binned in 1kb non overlaping windows</li> <li>WT_rep3_nanoT.rds contains the genomic BrdU signal profiles by 1kb non overlaping windows</li> <li>TeloLengthDataNanoT.rds contains all the telomeric sequences extracted from the experiments reported in the Figure 4 and S19 to S23 of the manuscript with the associated filtering information and nanotiming signal.</li> </ul> <p> </p>
Fig. 5 in Mitochondrial DNA diversity in the acanthocephalan Prosthenorchis elegans in Colombia based on cytochrome c oxidase I (COI) gene sequence
Fig. 5. Distribution and frequency of Prosthenorchis elegans haplotypes (A–F) and haplogroups (I–II) by locality and individual. URRAS: Unidad de Rescate y Rehabilitacíon de Animales Silvestres, Universidad Nacional de Colombia; AMVA: Area Metropolitana del Valle de Aburŕa; WCS: Wildlife Conservation Society-Colombia.
Fig. 4 in Mitochondrial DNA diversity in the acanthocephalan Prosthenorchis elegans in Colombia based on cytochrome c oxidase I (COI) gene sequence
Fig. 4. Phylogenetic tree obtained using Bayesian Inference (BI) and Maximum Likelihood (ML); node supports are provided for BI\ML. Outgroup taxa: Oncicola sp, AF417000; O. luehe = Oncicola luehe, JN710452; M. ingens = Macracanthorhynchus ingens, AF416997; M. hirudinaceus = Macracanthorhynchus hirudinaceus, FR856886; O. tortuous = Oligacanthorhynchus tortuous, AF416999.
Fig. 3 in Mitochondrial DNA diversity in the acanthocephalan Prosthenorchis elegans in Colombia based on cytochrome c oxidase I (COI) gene sequence
Fig. 3. Haplotype network of Prosthenorchis elegans. Network shows relationships among P.elegans haplotypes (A–F) recovered from Saguinus leucopus and Cebus albifrons based on 633 bp of COI. All branches are of unit length (one mutational step). Labeled open circles represent observed haplotypes; areas of circles are proportional to the number observed for each haplotype. Filled circles indicate inferred haplotypes not found among sampled individuals. Double lines indicate variable sites (49, 274 and 293) resulting in changes in amino acid. Haplogroups are identified.
Fig. 2 in Mitochondrial DNA diversity in the acanthocephalan Prosthenorchis elegans in Colombia based on cytochrome c oxidase I (COI) gene sequence
Fig. 2. External morphology of Prosthenorchis elegans via scanning electron microscopy (SEM). A. View of entire body of parasite. B. Proboscis armed with hooks.
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019) in Variability of the gene cyt b in the Korean field mouse Apodemus peninsulae Thomas, 1906 - a reservoir host of AMRV in the Khasansky District of Primorsky Krai
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019)
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.