We are working on custom designed assay for sequencing using Miseq V2 kits 300 cycles.
Following design we have used
Round 1 PCR
F-Primer
5’ ACACTCTTTCCCTACACGACGCTCTTCCGATCT-[locus specific sequence]
R-Primer
5’ GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT-[locus specific sequence]
Round 2 PCR
i5-
5'-AATGATACGGCGACCACCGAGATCTACAC-index-ACACTCTTTCCCTACACGACGCTCTTCCGATCT-3'
i7-
5'-CAAGCAGAAGACGGCATACGAGAT-index-GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT-3'
We are facing problem while demultiplexing. Along with the main i7 index read multiple other i7 index reads are getting paired against same i5 read. This decreases the overall coverage when files are demultiplexed using both i7 and i5. However when files are demultiplexed using only i5 reads the file coverage increases significantly.
Is it known problem with illumina platform?
Following design we have used
Round 1 PCR
F-Primer
5’ ACACTCTTTCCCTACACGACGCTCTTCCGATCT-[locus specific sequence]
R-Primer
5’ GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT-[locus specific sequence]
Round 2 PCR
i5-
5'-AATGATACGGCGACCACCGAGATCTACAC-index-ACACTCTTTCCCTACACGACGCTCTTCCGATCT-3'
i7-
5'-CAAGCAGAAGACGGCATACGAGAT-index-GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT-3'
We are facing problem while demultiplexing. Along with the main i7 index read multiple other i7 index reads are getting paired against same i5 read. This decreases the overall coverage when files are demultiplexed using both i7 and i5. However when files are demultiplexed using only i5 reads the file coverage increases significantly.
Is it known problem with illumina platform?