<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Czmil A</submitter><funding>Subcarpathian Center of Innovation</funding><funding>Oxford Nanopore technology: optimization of enzymes and analysis of genomic data for commercial applications</funding><funding>Foundation for Polish Science co-financed by the European Union under the European Regional Development Fund</funding><funding>Polish National Science Centre</funding><funding>Three-dimensional Human Genome structure at the population scale: computational algorithm and experimental validation for lymphoblastoid cell lines of selected families from 1000 Genomes Project</funding><funding>National Science Center</funding><funding>Identification of structural variants in the human genome using long fragments from next generation sequencing, based on Oxford Nanopore technology</funding><pagination>e13056</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8973472</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Next Generation Sequencing (NGS) techniques dominate today's landscape of genetics and genomics research. Though Illumina still dominates worldwide sequencing, Oxford Nanopore is one of the leading technologies currently being used by biologists, medics and geneticists across various applications. Oxford Nanopore is automated and relatively simple for conducting experiments, but generates gigabytes of raw data, to be processed by often ambiguous set of alternative bioinformatics command-line tools, and genomics frameworks which require a knowledge of bioinformatics to run.&lt;h4>Results&lt;/h4>We established an inter-collegiate collaboration across experimentalists and bioinformaticians in order to provide a novel bioinformatics tool, free for academics. This tool allows people without extensive bioinformatics knowledge to simply process their raw genome sequencing data. Currently, due to ICT resources' maintenance reasons, our server is only capable of handling small genomes (up to 15 Mb). In this paper, we introduce our tool, NanoForms: an intuitive and integrated web server for the processing and analysis of raw prokaryotic genome data, coming from Oxford Nanopore. NanoForms is freely available for academics at the following locations: http://nanoforms.tech (webserver) and https://github.com/czmilanna/nanoforms (GitHub source repository).</pubmed_abstract><journal>PeerJ</journal><pubmed_title>NanoForms: an integrated server for processing, analysis and assembly of raw sequencing data of microbial genomes, from Oxford Nanopore technology.</pubmed_title><pmcid>PMC8973472</pmcid><funding_grant_id>2018/02/X/NZ2/00622</funding_grant_id><funding_grant_id>05/PRZ/1/DG/PCI/2019</funding_grant_id><funding_grant_id>2019/35/O/ST6/02484</funding_grant_id><pubmed_authors>Sochacka-Pietal M</pubmed_authors><pubmed_authors>Wronski M</pubmed_authors><pubmed_authors>Strzalka D</pubmed_authors><pubmed_authors>Pietal M</pubmed_authors><pubmed_authors>Czmil A</pubmed_authors><pubmed_authors>Gawor J</pubmed_authors><pubmed_authors>Cmil M</pubmed_authors><pubmed_authors>Wolkowicz T</pubmed_authors><pubmed_authors>Plewczynski D</pubmed_authors><pubmed_authors>Czmil S</pubmed_authors></additional><is_claimable>false</is_claimable><name>NanoForms: an integrated server for processing, analysis and assembly of raw sequencing data of microbial genomes, from Oxford Nanopore technology.</name><description>&lt;h4>Background&lt;/h4>Next Generation Sequencing (NGS) techniques dominate today's landscape of genetics and genomics research. Though Illumina still dominates worldwide sequencing, Oxford Nanopore is one of the leading technologies currently being used by biologists, medics and geneticists across various applications. Oxford Nanopore is automated and relatively simple for conducting experiments, but generates gigabytes of raw data, to be processed by often ambiguous set of alternative bioinformatics command-line tools, and genomics frameworks which require a knowledge of bioinformatics to run.&lt;h4>Results&lt;/h4>We established an inter-collegiate collaboration across experimentalists and bioinformaticians in order to provide a novel bioinformatics tool, free for academics. This tool allows people without extensive bioinformatics knowledge to simply process their raw genome sequencing data. Currently, due to ICT resources' maintenance reasons, our server is only capable of handling small genomes (up to 15 Mb). In this paper, we introduce our tool, NanoForms: an intuitive and integrated web server for the processing and analysis of raw prokaryotic genome data, coming from Oxford Nanopore. NanoForms is freely available for academics at the following locations: http://nanoforms.tech (webserver) and https://github.com/czmilanna/nanoforms (GitHub source repository).</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-05-29T19:47:06.642Z</modification><creation>2025-04-05T07:15:35.97Z</creation></dates><accession>S-EPMC8973472</accession><cross_references><pubmed>35368340</pubmed><doi>10.7717/peerj.13056</doi></cross_references></HashMap>