Updated README.md

Author: rishvanth-kp

data/README.md

@@ -12,8 +12,9 @@ for the size of the chromosome. Not all chromosomes named in this file
 need to be used, but all chromosomes used in the CNV analysis must be
 present (with their sizes) in this file.
 
-## Bin definitions The CNV analysis begins with counts of reads in
-genomic bins. The bins are defined by have roughly equal size, but
+## Bin definitions 
+The CNV analysis begins with counts of reads in
+genomic bins. The bins are defined to have roughly equal size, but
 account for mappability, so the sizes vary slightly. We use files
 originally generated by scripts provided along with the publication:
 ```

test/README.md

@@ -1,6 +1,6 @@
 ## To test mapping simulated SMURF-seq reads to a small simulated genome
 A simulated reference genome `ref_sim.fa` has been indexed with BWA-MEM.
-`read_sim.fastq` contains simulated reads.
+`read_sim.fastq` contains simulated reads that align to `ref_sim.fa`.
 
 ## To test mapping simulated reads to the human genome
-`read_hg.fastq` contains simulated reads from the human genome.
+`read_hg.fastq` contains simulated reads that align to the human genome.