LiftOver alignments are used to map annotations from one human assembly to another one.
The subtracks of this track show two different types of liftOver: the first type was
created by the T2T consortium using the minimap2 aligner and strong filters;
it maps CHM13 coordinates to the human assemblies hg19 and hg38. The second
type was created by the UCSC Genome Browser Group using the lastz aligner and
relaxed filters; it maps CHM13 coordinates to hg19, hg38 and HG002 maternal
and HG002 paternal. (HG002 is one of the first Human Pangenome
Reference Consortium (HPRC) assemblies and both haplotypes
are available for this genome.)
The approaches of the two pipelines are different: T2T used the minimap2
aligner which outputs long alignments that do not require "chaining" of
alignments into longer ones, then removed alignments that go to other
chromosomes and removed all alignments to alternate haplotypes, fixes
(corrections to the assembly) and unplaced contig sequences. UCSC used the
lastz aligner with their chains/net pipeline (see below), and from these kept
all possible liftOver alignments, without a chromosome or sequence type
This means that the T2T alignments are tuned for high specificity, where
as the UCSC alignments are much more sensitive. The T2T alignments are
probably best used for mapping annotations to hg38 in automated pipelines and
in cases where the final processing on hg38 does not use alts/fixes/unplaced
sequences and when one wants to be sure that annotations that are mapped are
as reliable as possible. The UCSC alignments are probably best used for
manual inspection, when one is wondering "is there anything that could map to
this in hg38?" or when trying to get an idea where a particular sequence in
CHM13 could come from or when the final analysis is using the entire hg38
assembly, including alts/fixes/unplaced sequences.
Here are some examples to illustrate the differences:
- Example 1: The acrocentric
arms of chromosomes 13, 14, 15, 21, 22 and Y where not sequenced in hg38 at all but they are
present in CHM13. The T2T liftOver shows that little is mappable there, as
the sequence is entirely new. The UCSC liftOver pipeline shows a lot of
alignable pieces in them, because these repeats and rDNA sequences have
similar copies in hg38. It depends on the particular analysis which approach is more appropriate.
A note on genes: As the link above shows, even though the sequence is new,
the T2T group mapped hg38 Gencode 35 gene models into these regions using
CAT/LiftOff. This is because CAT and liftOff are using approaches for their
lifting of genes / mapping that are not based on the liftOver alignments but sequence homology,
like the UCSC liftOver pipeline.
- Example 2: The ABO gene in CHM13
is a longer haplotype than in hg38. In the T2T liftOver alignments, it looks as if the sequence
was entirely missing in hg38. The UCSC
liftOver alignments show that this sequence has been patched post-release into hg38 via chr9_KN196479v1_fix.
Analyses ignoring alts/fixes/unplaced sequences should use the T2T alignments here.
Also, we created dot plots from these alignments as an experiment to further demonstrate the differences betweem them:
The track displays boxes joined together by either single or double lines,
with the boxes represent aligning regions, single lines indicating gaps that
are largely due to a deletion in the CHM13 v2.0 assembly or an insertion in
the GRCh38 or GRCh37, and double lines representing more complex gaps that
involve substantial sequence in both assembly.
LiftOver chain file downloads
One-to-one liftOver chain files to and from GRCh38/hg38 and GRCh37/hg19 are available here:
The mask file for GRCh38/hg38
T2T GRCh38/hg38 pre-processing
To prevent ambiguous alignments, all false duplications, as determined by the Genome in a Bottle Consortium
(GCA_000001405.15_GRCh38_GRC_exclusions_T2Tv2.bed), as well as the GRCh38 modeled centromeres,
were masked from the GRCh38/hg38 primary assembly. In addition, unlocalized and unplaced (random) contigs were removed.
T2T GRCh37/hg19 pre-processing
Unlocalized and unplaced (random) contigs were removed from the GRCh37/hg19 assembly.
T2T Alignment and Chain Creation
For the minimap2-based pipeline, the initial chain file was generated using
nf-LO v1.5.1 with
minimap2 v2.24 alignments. These chains were then split at all locations that contained unaligned segments greater than 1kbp or gaps greater than 10kbp. Split chain files were then converted to PAF format with extended CIGAR strings using chaintools (https://doi.org/10.5281/zenodo.6342391, v0.1), and alignments between nonhomologous chromosomes were removed. The trim-paf operation of rustybam (https://zenodo.org/record/6342176, v0.1.29) was next used to remove overlapping alignments in the query sequence, and then the target sequence, to create 1:1 alignments. PAF alignments were converted back to the chain format with paf2chain commit f68eeca, and finally, chaintools was used to generate the inverted chain file.
Full commands with parameters used were:
nextflow run main.nf --source GRCh38.fa --target chm13v2.0.fasta --outdir dir -profile local --aligner minimap2
python chaintools/src/split.py -c input.chain -o input-split.chain
python chaintools/src/to_paf.py -c input-split.chain -t target.fa -q query.fa -o input-split.paf
awk '$1==$6' input-split.paf | rb break-paf --max-size 10000 | rb trim-paf -r | rb invert | rb trim-paf -r | rb invert > out.paf
paf2chain -i out.paf > out.chain
python chaintools/src/invert.py -c out.chain -o out_inverted.chain
uses dynamic programming and the CIGAR string to find an optimal
splitting point between overlapping alignments in the query sequence. It
starts its trimming with the largest overlap and then recursively trims
Results were validated by using chaintools to confirm that there were no
overlapping sequences with respect to both CHM13v2.0 and GRCh38 in the
released chain file. In addition, trimmed alignments were visually inspected
with SafFire to confirm their quality.
UCSC pipeline methods
The UCSC pipeline is driven by DoBlastzChainNet.pl, a script used for all current human
assemblies and hundreds of other genome comparisons. It has been developed over
20 years and goes through these steps:
Alignment and chaining of alignments: The query genome was
aligned to target genome with lastz. The resulting alignments
were converted into axt format using the lavToAxt
program. The axt alignments were fed into axtChain, which organizes all
alignments between a single query chromosome and a single
target chromosome into a group and creates a kd-tree out
of the gapless subsections (blocks) of the alignments. A dynamic program
was then run over the kd-trees to find the maximally scoring chains of these
Netting of alignments:
Chains were derived from lastz alignments, using the methods
described on the chain tracks description pages, and sorted with the
highest-scoring chains in the genome ranked first. The program
chainNet was then used to place the chains one at a time, trimming them as
necessary to fit into sections not already covered by a higher-scoring chain.
During this process, a natural hierarchy emerged in which a chain that filled
a gap in a higher-scoring chain was placed underneath that chain. The program
netSyntenic was used to fill in information about the relationship between
higher- and lower-level chains, such as whether a lower-level
chain was syntenic or inverted relative to the higher-level chain.
The program netClass was then used to fill in how much of the gaps and chains
contained Ns (sequencing gaps) in one or both species and how much
was filled with transposons inserted before and after the two organisms
LiftOver alignment extraction: Finally, the chains referred to by the top-level nets are used
to create a liftOver alignment file using netChainSubset and chainStitchId.
The T2T v1_nflo liftOver chains were generated by Nae-Chyun
Chen<email@example.com> and Mitchell
Vollger<firstname.lastname@example.org>. The UCSC liftOver chains and the dot-plots
were created by Hiram Clawson.
lastz was developed by Robert Harris, Pennsylvania State University.
The axtChain program was developed at the University of California at
Santa Cruz by Jim Kent with advice from Webb Miller and David Haussler.
The browser display and database storage of the chains and nets were created
by Robert Baertsch and Jim Kent.
The chainNet, netSyntenic, and netClass programs
were developed at the University of California
Santa Cruz by Jim Kent.
Nurk S, Koren S, Rhie A, Rautiainen M, et al. The complete sequence of a human genome. bioRxiv, 2021.
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Ph.D. Thesis, The Pennsylvania State University
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Scoring pairwise genomic sequence alignments.
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Proc Natl Acad Sci U S A. 2003 Sep 30;100(20):11484-9.
PMID: 14500911; PMC: PMC208784
Schwartz S, Kent WJ, Smit A, Zhang Z, Baertsch R, Hardison RC,
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