Technical note Open Access
Nicouleau, Michael; Durcan, Thomas M.
{ "files": [ { "links": { "self": "https://zenodo.org/api/files/d67adee8-3d6a-4ec0-b125-2a1b5b4024b6/EDDU-014-01_Sequencing%20analysis%20overview_v1.0.pdf" }, "checksum": "md5:02e766b62d55ec2354f65010e2a14bbb", "bucket": "d67adee8-3d6a-4ec0-b125-2a1b5b4024b6", "key": "EDDU-014-01_Sequencing analysis overview_v1.0.pdf", "type": "pdf", "size": 3033775 } ], "owners": [ 61784 ], "doi": "10.5281/zenodo.3810825", "stats": { "version_unique_downloads": 127.0, "unique_views": 163.0, "views": 175.0, "version_views": 175.0, "unique_downloads": 127.0, "version_unique_views": 163.0, "volume": 397424525.0, "version_downloads": 131.0, "downloads": 131.0, "version_volume": 397424525.0 }, "links": { "doi": "https://doi.org/10.5281/zenodo.3810825", "conceptdoi": "https://doi.org/10.5281/zenodo.3810824", "bucket": "https://zenodo.org/api/files/d67adee8-3d6a-4ec0-b125-2a1b5b4024b6", "conceptbadge": "https://zenodo.org/badge/doi/10.5281/zenodo.3810824.svg", "html": "https://zenodo.org/record/3810825", "latest_html": "https://zenodo.org/record/3810825", "badge": "https://zenodo.org/badge/doi/10.5281/zenodo.3810825.svg", "latest": "https://zenodo.org/api/records/3810825" }, "conceptdoi": "10.5281/zenodo.3810824", "created": "2020-05-07T02:06:57.650498+00:00", "updated": "2020-06-19T21:12:45.994154+00:00", "conceptrecid": "3810824", "revision": 3, "id": 3810825, "metadata": { "access_right_category": "success", "doi": "10.5281/zenodo.3810825", "description": "<p>Sanger sequencing is a method of DNA sequencing that is based on the selective incorporation of chain-terminating dideoxynucleotides by DNA polymerase during in vitro DNA replication.</p>\n\n<p>Sanger sequencing analysis software packages are used for base calling (process of assigning <a href=\"https://en.wikipedia.org/wiki/Nucleobase\">nucleobases</a> to <a href=\"https://en.wikipedia.org/wiki/Chromatogram\">chromatogram</a> peaks), sequence alignment, trace visualization and variant detection.</p>\n\n<p>In this protocol, we describe our method used for analyzing sequence data obtained with our Applied Biosystems SeqStudio Genetic Analyzer instrument and analyzed using SnapGene software.</p>", "language": "eng", "title": "Sequencing Analysis Guide", "license": { "id": "CC-BY-4.0" }, "relations": { "version": [ { "count": 1, "index": 0, "parent": { "pid_type": "recid", "pid_value": "3810824" }, "is_last": true, "last_child": { "pid_type": "recid", "pid_value": "3810825" } } ] }, "communities": [ { "id": "sgc-opennotebook" } ], "version": "V1.0", "keywords": [ "sequencing", "snapgene", "DNA analysis" ], "publication_date": "2020-05-07", "creators": [ { "affiliation": "MNI, McGill University", "name": "Nicouleau, Michael" }, { "affiliation": "MNI, McGill University", "name": "Durcan, Thomas M." } ], "access_right": "open", "resource_type": { "subtype": "technicalnote", "type": "publication", "title": "Technical note" }, "related_identifiers": [ { "scheme": "doi", "identifier": "10.5281/zenodo.3810824", "relation": "isVersionOf" } ] } }
All versions | This version | |
---|---|---|
Views | 175 | 175 |
Downloads | 131 | 131 |
Data volume | 397.4 MB | 397.4 MB |
Unique views | 163 | 163 |
Unique downloads | 127 | 127 |