Aleksandr Sidoruk
YOU?
Author Swipe
View article: Peer Review #2 of "Prioritisation of structural variant calls in cancer genomes (v0.2)"
Peer Review #2 of "Prioritisation of structural variant calls in cancer genomes (v0.2)" Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data.In this paper we describe a tiered prioritisat…
View article: Peer Review #3 of "Prioritisation of structural variant calls in cancer genomes (v0.1)"
Peer Review #3 of "Prioritisation of structural variant calls in cancer genomes (v0.1)" Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data.In this paper we describe a tiered prioritisat…
View article: Peer Review #2 of "Prioritisation of structural variant calls in cancer genomes (v0.1)"
Peer Review #2 of "Prioritisation of structural variant calls in cancer genomes (v0.1)" Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data.In this paper we describe a tiered prioritisat…
View article: Peer Review #1 of "Prioritisation of structural variant calls in cancer genomes (v0.1)"
Peer Review #1 of "Prioritisation of structural variant calls in cancer genomes (v0.1)" Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data.In this paper we describe a tiered prioritisat…
View article: Peer Review #3 of "Prioritisation of structural variant calls in cancer genomes (v0.2)"
Peer Review #3 of "Prioritisation of structural variant calls in cancer genomes (v0.2)" Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data.In this paper we describe a tiered prioritisat…
View article: Prioritisation of structural variant calls in cancer genomes
Prioritisation of structural variant calls in cancer genomes Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data. In this paper we describe a tiered prioritisa…
View article: Peer Review #1 of "Prioritisation of structural variant calls in cancer genomes (v0.2)"
Peer Review #1 of "Prioritisation of structural variant calls in cancer genomes (v0.2)" Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data.In this paper we describe a tiered prioritisat…
View article: Prioritisation of Structural Variant Calls in Cancer Genomes
Prioritisation of Structural Variant Calls in Cancer Genomes Open
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data. In this paper we describe a tiered prioritisa…