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Additional file 2

This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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Abstract

Description of tailcurve (nucleotide proportion at individual cycles along the sequence read). With perfect random fragmentation, a given position and its associated base calls (consensus and variant) should be represented at multiple sequencing cycles. With high coverage, a particular base call will be present for that position at all or most cycles. Example: for a sequencing module of 25 cycles with several hundred (24 shown) overlapping reads covering the highlighted position, all the cycles are represented by 'G', with variant reads producing the 'T' at a handful of cycles (potential variant).