| Name | NGSFeatGen |
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| Aliases | Next Generation Sequencing Feature Generation |
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| Description | This software is a framework for predicting true reads from the next generation sequencing data. This software generates several key features: observed count, estimate true count, loglikelihood with entropy penalty, loglikelihood ratio, expectation matching score, and specific correction coefficient. |
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| Type | Tool |
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| Main Institutes of management | Computational Biology Research Center (CBRC), National Institute of Advanced Industrial Science and Technology (AIST) |
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| Country of the Institute | Japan |
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| URL of the site | - |
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| Interface | CUI |
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| Input | |
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| Output | |
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| Input example | You can run recount by executing the wrapper written in Perl.The command is simply:perl ngsfeatgen.pl <input> |
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| Keyword | NGS|Classification|Illumina|Solexa |
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| Amount of the all data for download（Mbyte） | Method to obtain the all data. | |
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| External resources (databases) in building the product. | None |
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| Data type | DNA-sequence NGS |
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| Biological species in the main concern | All species |
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| Conditions of use | None |
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| Frequency of updates (in last two years) | 0 time/year |
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| Last date of updates (date of confirmation) | 2010/03/22 (2019/07/08) |
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| Main IDs used in the products | None |
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| How to make a link to get access to each IDs. | None |
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| external databases to which this database/tool have links | None |
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| Published papers (PubMed IDs) | pmid:23349826 | pmid:23413433 |
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| Operational Status | Closed |
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