diff --git a/README.md b/README.md
index b375278..0d40147 100644
--- a/README.md
+++ b/README.md
@@ -12,7 +12,7 @@ cd minimap2 && make
./minimap2 -x map-ont -d MT-human-ont.mmi test/MT-human.fa
./minimap2 -a MT-human-ont.mmi test/MT-orang.fa > test.sam
# use presets (no test data)
-./minimap2 -ax map-pb ref.fa pacbio.fq.gz > aln.sam # PacBio genomic reads
+./minimap2 -ax map-pb ref.fa pacbio.fq.gz > aln.sam # PacBio CLR genomic reads
./minimap2 -ax map-ont ref.fa ont.fq.gz > aln.sam # Oxford Nanopore genomic reads
./minimap2 -ax map-hifi ref.fa pacbio-ccs.fq.gz > aln.sam # PacBio HiFi/CCS genomic reads
./minimap2 -ax sr ref.fa read1.fa read2.fa > aln.sam # short genomic paired-end reads
@@ -139,13 +139,13 @@ parameters at the same time. The default setting is the same as `map-ont`.
#### Map long noisy genomic reads
```sh
-minimap2 -ax map-pb ref.fa pacbio-reads.fq > aln.sam # for PacBio subreads
+minimap2 -ax map-pb ref.fa pacbio-reads.fq > aln.sam # for PacBio CLR reads
minimap2 -ax map-ont ref.fa ont-reads.fq > aln.sam # for Oxford Nanopore reads
```
The difference between `map-pb` and `map-ont` is that `map-pb` uses
homopolymer-compressed (HPC) minimizers as seeds, while `map-ont` uses ordinary
minimizers as seeds. Emperical evaluation suggests HPC minimizers improve
-performance and sensitivity when aligning PacBio reads, but hurt when aligning
+performance and sensitivity when aligning PacBio CLR reads, but hurt when aligning
Nanopore reads.
#### Map long mRNA/cDNA reads
@@ -206,7 +206,7 @@ strand field. In this case, each line indicates an oriented junction.
#### Find overlaps between long reads
```sh
-minimap2 -x ava-pb reads.fq reads.fq > ovlp.paf # PacBio read overlap
+minimap2 -x ava-pb reads.fq reads.fq > ovlp.paf # PacBio CLR read overlap
minimap2 -x ava-ont reads.fq reads.fq > ovlp.paf # Oxford Nanopore read overlap
```
Similarly, `ava-pb` uses HPC minimizers while `ava-ont` uses ordinary