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660 results for “Genome assemblies”

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dryad36/100

Ion Torrent data for the genome assembly and phylogenomic placement of mitochondrial genomes with a focus on houndsharks (Chondrichthyes: Triakidae)

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publicFeb 2025View details →
dryad36/100

Annotated genome assemblies for Geoscapheus dilatatus, Panesthia cribrata and Neogeoscapheus hanni

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publicFeb 2024View details →
dryad36/100

Accurate, scalable, and fully automated inference of species trees from raw genome assemblies using ROADIES

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publicJan 2025View details →
dryad36/100

Genome sequence assembly and annotation of MATA and MATB strains of <em>Yarrowia lipolytica</em>

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publicOct 2025View details →
dryad36/100

A pan-cetacean MHC amplicon sequencing panel developed and evaluated in combination with genome assemblies

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publicFeb 2024View details →
dryad36/100

FC309 genome assembly and annotation files

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publicMar 2025View details →
dryad36/100

Data from: A high-quality genome assembly for a desert-adapted rodent, Merriam’s kangaroo rat (Dipodomys merriami)

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publicApr 2025View details →
dryad36/100

Long read genome assembly of Automeris io (Lepidoptera: Saturniidae) an emerging model for the evolution of deimatic displays

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publicFeb 2024View details →
dryad36/100

A chromosome-scale high-contiguity genome assembly of the threatened cheetah (Acinonyx jubatus)

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publicJan 2023View details →
dryad36/100

Data from: Genome assembly of a diversity panel of Chenopodium quinoa

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publicOct 2024View details →
dryad36/100

De novo genome assembly of human cell line CHM13 nanopore ultra-long reads using Shasta

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publicMay 2022View details →
dryad36/100

A highly contiguous genome assembly for the California quail (Callipepla californica)

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publicMay 2023View details →
dryad36/100

Whole genome assembly and annotation of the King Angelfish (Holacanthus passer) gives insight into the evolution of marine fishes of the Tropical Eastern Pacific

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publicNov 2023View details →
zenodo32/100

Nanopore long reads enable the first complete genome assembly of a Malaysian Vibrio parahaemolyticus isolate bearing the pVa plasmid associated with acute hepatopancreatic necrosis disease

<p>Supplemental File 1: Main genome assemblies (Unpolished Flye assembly, Polished Flye assembly, Unicycler Hybrid Assembly and Unicycler Illumina-only assembly) generated in this study for comparison and their BUSCO output.</p> <p>Supplemental File 2: Phyre2 protein modelling output of the putative MVP1 TcdA toxin</p> <p>Supplemental File 3: Phyre2 protein modelling output of the putative MVP1 TcdB toxin</p> <p>Supplemental File 4: Phyre2 protein modelling output of the putative MVP1 TccC toxin</p> <p>Supplemental File 5: InterProScan output of the NCBI-predicted MVP1 proteome.</p> <p>Supplemental Table 1: NCBI BlastN output using the <em>fuc</em> genes of <em>Vibrio parahaemolyticus</em> MVP1 as the query to search against the Vibrio reference WGS database as of 21 Oct 2019</p>

opencc-by-4.0Dec 2019View details →
zenodo32/100

DAS Tool 1.1.2 genome binning of the CAMI 2 Mouse Gut Toy data set, samples 0-63, gold standard pooled assembly

Genome binning of the gold standard pooled assembly. Refinement of the binning output of MaxBin 2.2.7, MetaBAT 2.12.1, CONCOCT 1.0.0, and DAS Tool 1.1.2.<br><strong>Software: </strong>DAS Tool<br><strong>SoftwareVersion: </strong>1.1.2<br><strong>DataURL: </strong> https://data.cami-challenge.org/participate<br><strong>SoftwareURL:</strong> https://github.com/cmks/DAS_Tool<br><strong>DockerImage:</strong> cami/das_tool:1.1.2<br><strong>IsBiobox:</strong> No<br><strong>ShortReadsUsed:</strong> True<br><strong>LongReadsUsed:</strong> False<br><strong>CommandUsed:</strong> DAS_Tool -i binning_concoct1.0.0,binning_maxbin2.2.7,binning_metabat2.12.1 -c anonymous_gsa_pooled.fasta -o output --search_engine diamond

opencc-by-4.0Jan 2020View details →
zenodo32/100

CONCOCT 1.0.0 genome binning of the CAMI 2 Mouse Gut Toy data set, samples 0-63, gold standard pooled assembly

Genome binning of the gold standard pooled assembly <br><strong>Software: </strong>CONCOCT<br><strong>SoftwareVersion: </strong>1.0.0<br><strong>DataURL: </strong> https://data.cami-challenge.org/participate<br><strong>SoftwareURL:</strong> https://github.com/BinPro/CONCOCT<br><strong>DockerImage:</strong> quay.io/biocontainers/concoct:1.0.0--py37h88e4a8a_5<br><strong>IsBiobox:</strong> No<br><strong>ShortReadsUsed:</strong> True<br><strong>LongReadsUsed:</strong> False<br><strong>CommandUsed:</strong> for i in {0..63}; do bowtie2 -q --threads 30 --fr -x anonymous_gsa_pooled.fasta --interleaved sample_${i}/anonymous_reads.fq -S anonymous_reads_sample_${i}.sam ; done<br>for i in {0..63}; do samtools view -b sample_${i}.sam -o anonymous_reads_sample_${i}.bam &amp; done<br>for i in {0..63}; do samtools sort anonymous_reads_sample_${i}.bam -o anonymous_reads_sample_${i}.sorted.bam ; done<br>for i in {0..63}; do samtools index anonymous_reads_sample_${i}.sorted.bam ; done<br>cut_up_fasta.py anonymous_gsa_pooled.fasta -c 10000 -o 0 --merge_last -b contigs_10K.bed &gt; contigs_10K.fa<br>concoct_coverage_table.py contigs_10K.bed /host/benchmarking/fmeyer/output/bowtie2/mouse_gut/sorted_bam/anonymous_reads_sample_*.sorted.bam &gt; coverage_table.tsv<br>concoct --composition_file contigs_10K.fa --coverage_file coverage_table.tsv -b<br>merge_cutup_clustering.py clustering_gt1000.csv &gt; clustering_merged.csv

opencc-by-4.0Jan 2020View details →
zenodo32/100

MaxBin 2.2.7 genome binning of the CAMI 2 Mouse Gut Toy data set, samples 0-63, gold standard pooled assembly

Genome binning of the gold standard pooled assembly <br><strong>Software: </strong>MaxBin<br><strong>SoftwareVersion: </strong>2.2.7<br><strong>DataURL: </strong> https://data.cami-challenge.org/participate<br><strong>SoftwareURL:</strong> https://sourceforge.net/projects/maxbin/<br><strong>DockerImage:</strong> cami/maxbin:2.2.7<br><strong>IsBiobox:</strong> No<br><strong>ShortReadsUsed:</strong> True<br><strong>LongReadsUsed:</strong> False<br><strong>CommandUsed:</strong> run_MaxBin.pl -thread 16 -contig anonymous_gsa_pooled.fasta -out output -reads sample_0/reads/anonymous_reads.fq -reads2 sample_1/reads/anonymous_reads.fq -reads3 sample_2/reads/anonymous_reads.fq -reads4 sample_3/reads/anonymous_reads.fq -reads5 sample_4/reads/anonymous_reads.fq -reads6 sample_5/reads/anonymous_reads.fq -reads7 sample_6/reads/anonymous_reads.fq -reads8 sample_7/reads/anonymous_reads.fq -reads9 sample_8/reads/anonymous_reads.fq -reads10 sample_9/reads/anonymous_reads.fq -reads11 sample_10/reads/anonymous_reads.fq -reads12 sample_11/reads/anonymous_reads.fq -reads13 sample_12/reads/anonymous_reads.fq -reads14 sample_13/reads/anonymous_reads.fq -reads15 sample_14/reads/anonymous_reads.fq -reads16 sample_15/reads/anonymous_reads.fq -reads17 sample_16/reads/anonymous_reads.fq -reads18 sample_17/reads/anonymous_reads.fq -reads19 sample_18/reads/anonymous_reads.fq -reads20 sample_19/reads/anonymous_reads.fq -reads21 sample_20/reads/anonymous_reads.fq -reads22 sample_21/reads/anonymous_reads.fq -reads23 sample_22/reads/anonymous_reads.fq -reads24 sample_23/reads/anonymous_reads.fq -reads25 sample_24/reads/anonymous_reads.fq -reads26 sample_25/reads/anonymous_reads.fq -reads27 sample_26/reads/anonymous_reads.fq -reads28 sample_27/reads/anonymous_reads.fq -reads29 sample_28/reads/anonymous_reads.fq -reads30 sample_29/reads/anonymous_reads.fq -reads31 sample_30/reads/anonymous_reads.fq -reads32 sample_31/reads/anonymous_reads.fq -reads33 sample_32/reads/anonymous_reads.fq -reads34 sample_33/reads/anonymous_reads.fq -reads35 sample_34/reads/anonymous_reads.fq -reads36 sample_35/reads/anonymous_reads.fq -reads37 sample_36/reads/anonymous_reads.fq -reads38 sample_37/reads/anonymous_reads.fq -reads39 sample_38/reads/anonymous_reads.fq -reads40 sample_39/reads/anonymous_reads.fq -reads41 sample_40/reads/anonymous_reads.fq -reads42 sample_41/reads/anonymous_reads.fq -reads43 sample_42/reads/anonymous_reads.fq -reads44 sample_43/reads/anonymous_reads.fq -reads45 sample_44/reads/anonymous_reads.fq -reads46 sample_45/reads/anonymous_reads.fq -reads47 sample_46/reads/anonymous_reads.fq -reads48 sample_47/reads/anonymous_reads.fq -reads49 sample_48/reads/anonymous_reads.fq -reads50 sample_49/reads/anonymous_reads.fq -reads51 sample_50/reads/anonymous_reads.fq -reads52 sample_51/reads/anonymous_reads.fq -reads53 sample_52/reads/anonymous_reads.fq -reads54 sample_53/reads/anonymous_reads.fq -reads55 sample_54/reads/anonymous_reads.fq -reads56 sample_55/reads/anonymous_reads.fq -reads57 sample_56/reads/anonymous_reads.fq -reads58 sample_57/reads/anonymous_reads.fq -reads59 sample_58/reads/anonymous_reads.fq -reads60 sample_59/reads/anonymous_reads.fq -reads61 sample_60/reads/anonymous_reads.fq -reads62 sample_61/reads/anonymous_reads.fq -reads63 sample_62/reads/anonymous_reads.fq -reads64 sample_63/reads/anonymous_reads.fq

opencc-by-4.0Jan 2020View details →
zenodo32/100

Eigen scores for human genome assembly GRCh38 Part 1 (Chr12 - Chr22)

<p>Eigen is a spectral approach to the functional annotation of genetic variants in coding and noncoding regions. Eigen makes use of a variety of functional annotations in both coding and noncoding regions (such as protein function scores, evolutionary conservation scores, and epigenetic annotations from ENCODE and Roadmap Epigenomics projects), and combines them into one single measure of functional importance. Eigen is an unsupervised approach, and, unlike many existing methods, is not based on any labelled training data. Eigen produces estimates of predictive accuracy for each functional annotation score, and subsequently uses these estimates of accuracy to derive the aggregate functional score for variants of interest as a weighted linear combination of individual annotations.</p>

opencc-by-4.0Dec 2018View details →
zenodo32/100

Eigen scores for human genome assembly GRCh38 Part 2 (Chr6 - Chr11)

<p>Eigen is a spectral approach to the functional annotation of genetic variants in coding and noncoding regions. Eigen makes use of a variety of functional annotations in both coding and noncoding regions (such as protein function scores, evolutionary conservation scores, and epigenetic annotations from ENCODE and Roadmap Epigenomics projects), and combines them into one single measure of functional importance. Eigen is an unsupervised approach, and, unlike many existing methods, is not based on any labelled training data. Eigen produces estimates of predictive accuracy for each functional annotation score, and subsequently uses these estimates of accuracy to derive the aggregate functional score for variants of interest as a weighted linear combination of individual annotations.</p>

opencc-by-4.0Jun 2019View details →
zenodo32/100

Demo dataset for diploid genome assembly pipeline

<p>Small-scale demo data to test the diploid genome assembly pipeline. The tar archive contains PacBio HiFi/CCS and Strand-seq reads, plus a reduced genome reference. For instructions how to run the demo data, please refer to the documentation hosted in the pipeline repository (see related identifiers).</p>

opencc-by-4.0Apr 2020View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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Your academic CV and NIH biosketch

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