If you are interested in participating this Coordination Action please contact us!
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| public:loadedtestcases:tc2 [2012/09/12 09:04] – [Animalss] andreas | public:loadedtestcases:tc2 [2019/02/12 09:04] (current) – external edit 127.0.0.1 | ||
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| ====NGSGAPS==== | ====NGSGAPS==== | ||
| ==Test Case Class== | ==Test Case Class== | ||
| - | ====Animals==== | + | ====Plants (Animals)==== |
| ==Contact person== | ==Contact person== | ||
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| Project should focus on the generation of software that first of all allows for a rapid assessment of the quality of the sequence data. New ways for mapping short reads to a reference genome should be designed, allowing for more flexible gap options, variable assembling parameters that rely on the local context of the genomic region and iterative read mapping. | Project should focus on the generation of software that first of all allows for a rapid assessment of the quality of the sequence data. New ways for mapping short reads to a reference genome should be designed, allowing for more flexible gap options, variable assembling parameters that rely on the local context of the genomic region and iterative read mapping. | ||
| ==Discussion== | ==Discussion== | ||
| - | nd | + | LF: identifying large structural variations with unfinished genomes is rather difficult. What is possible is to remap the paired-end or better the mate-pair reads and use that information. There are a number of tools able to do that: breakdancer, |
| + | Ken Chen, Aaron Quinlan, gasv@cs.brown.edu, | ||
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