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Workflow NGS : RNAseq workflow part 1 from Tophat t... (1)

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Remove duplicates from Tophat BAM output files and filter

Created: 2014-03-04 | Last updated: 2014-06-10

Credits: User Ylebras

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Pack Astronomy Taverna 2.5 starter pack


Created: 2014-03-03 17:02:08 | Last updated: 2014-03-03 17:16:57

This is a set of small snippets using Astronomy Taverna. The purpose of this pack is to make the design and development of astronomy Virtual Observatory workflows easier, learning by the example. Additionally, you can find other Astronomy related workflows and snippets related to general functionalities of Taverna. 

45 items in this pack

Comments: 0 | Viewed: 96 times | Downloaded: 26 times

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Blob LOGS

Created: 2014-03-02 22:34:21 | Last updated: 2014-04-18 00:54:19

Credits: User cecilia Amaya

License: Creative Commons Attribution-Share Alike 3.0 Unported License

ESTRUCTURAS CREADAS PARA LOGS:APACHE-ACCESOAPACHE-ERROSENDMAILPOSFIXKERNELSNORT FULLSNORT FAST

File type: application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

Comments: 0 | Viewed: 56 times | Downloaded: 19 times

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Workflow NGS : Mini assembly from FastQ files using... (1)

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Assemble FastQ reads with minia

Created: 2014-02-28 | Last updated: 2014-06-10

Credits: User Ylebras

Workflow pubmed abstracts from pathways (1)

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Extraction of the abstracts from pubmed pubblications related to the pathways involving the input genes

Created: 2014-02-28

Credits: User Massimo La Rosa User Antonino Fiannaca

Attributions: Workflow NCBI Gi to Kegg Pathway Descriptions Workflow Pathway to Pubmed

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Workflow NGS : Filter contamination in raw reads by ID (1)

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Filter FastQ sequences by ID

Created: 2014-02-28 | Last updated: 2014-06-10

Credits: User Ylebras

Uploader

Workflow NGS : Bowtie2 using built-in genome to dep... (1)

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Reads mapping using a built-in genome from your history, then generate pileup, base coverage, depth of coverage and summary statistics

Created: 2014-02-28 | Last updated: 2014-06-10

Credits: User Ylebras

Uploader

Workflow NGS : Bowtie2 with a genome in fasta forma... (1)

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Reads mapping using a reference genome in fasta format from your history, then generate pileup, base coverage, depth of coverage and summary statistics

Created: 2014-02-28 | Last updated: 2014-06-10

Credits: User Ylebras

Uploader

Workflow NGS : Coverage determination and visualiza... (1)

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From a BAM file and a reference genome fasta file, calculate the depth of coverage and generate pileup, interval, Base coverage as Summary statistics

Created: 2014-02-28 | Last updated: 2014-06-10

Credits: User Ylebras

Uploader

Workflow NGS : flanking SNP regions (1)

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Flank SNP regions using interval format file and a fasta reference file

Created: 2014-02-28 | Last updated: 2014-06-10

Credits: User Ylebras

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