find-deletion-q1

Question

You are given shallow paired-end whole genome sequencing FASTQ files (find.deletion.r1.fq.gz, find.deletion.r2.fq.gz) simulated from a chromosome of the human genome hg38 which contains a large deletion. Your task is to identify the approximate coordinates of this deletion relative to the reference genome. Report the chromosome, the start coordinate, and the end coordinate of the deletion, with both coordinates rounded to the nearest 100,000 bases. Format your answer as chr:start-end. For example: chr1:10000000-10300000.

Inferred answer

chr22:20000000-21000000Uniquely inferred from submitted scores.

Domain

Genomics

Question style

Synthetic/Augmented Data

An answer can be uniquely inferred for 54 of 100 questions from submitted scores. Green: correct · Red: incorrect. For questions without a uniquely determined answer: Blue: matches prediction · Orange: differs from prediction. These are inferred answer checks, not official per-question grades.