Seemingly similar cells often have significantly different genomes. This
is often true of cancer cells, for example, which may differ one from
another even within a small tumor sample, as genetic mutations within
the cells spread in staccato-like bursts. Detailed knowledge of these
mutations, called copy number variations, in individual cells can point
to specific treatment regimens.
The problem is that current techniques for acquiring this knowledge
are difficult and produce unreliable results. Today, scientists at Cold
Spring Harbor Laboratory (CSHL) publish a new interactive analysis
program called Gingko that reduces the uncertainty of single-cell
analysis and provides a simple way to visualize patterns in copy number
mutations across populations of cells.
The open-source software, which is freely available online, will
improve scientists' ability to study this important type of genetic
anomaly and could help clinicians better target medications based on
cells' specific mutation profiles. The software is described online
today in Nature Methods.
Mutations come in many forms. For example, in the most common type of
mutation, variations may exist among individual people—or cells—at a
single position in a DNA sequence. Another common mutation is a copy
number variation (CNV), in which large chunks of DNA are either deleted
from or added to the genome. When there are too many or too few copies
of a given gene or genes, due to CNVs, disease can occur. Such mutations
have been linked not only with cancer but a host of other illnesses,
including autism and schizophrenia.
Researchers can learn a lot by analyzing CNVs in bulk samples—from a
tumor biopsy, for example—but they can learn more by investigating CNVs
in individual cells.
"You may think that every cell in a tumor would be the same, but that's
actually not the case," says CSHL Associate Professor Michael Schatz.
"We're realizing that there can be a lot of changes inside even a
single tumor," says Schatz. "If you're going to treat cancer, you need
to diagnose exactly what subclass of cancer you have." Simultaneously
employing different drugs to target different cancer subclasses could
prevent remission, scientists have proposed.
One powerful single-cell analytic technique for exploring CNV is
whole genome sequencing. The challenge is that, before sequencing can be
done, the cell's DNA has to be amplified many times over. This process
is rife with errors, with some arbitrary chunks of DNA being amplified
more than others. In addition, because many labs use their own software
to examine CNVs, there is little consistency in how researchers analyze
their results.
To address these two challenges, Schatz and his colleagues created
Gingko. The interactive, web-based program automatically processes
sequence data, maps the sequences to a reference genome, and creates CNV
profiles for every cell that can then be viewed with a user-friendly
graphical interface. In addition, Gingko constructs phylogenetic trees
based on the profiles, allowing cells with similar copy number mutations
to be grouped together.
Importantly, Gingko, which Schatz and his colleagues validated by
reproducing the findings of five major single-cell studies, also
analyzes patterns in the sequence reads in order to recognize, and
greatly reduce, amplification errors.
Schatz and his team named their software after the gingko tree, which
has many well-documented therapeutic benefits. "We like to think our
Gingko 'trees' will provide benefits as well," says Schatz, referring to
the graphical way that CNV changes are represented by analysts. Right
now, CNV is not a commonly used diagnostic measurement in the clinic.
"We're looking into the best way of collecting samples, analyzing them,
and informing clinicians about the results," says Schatz. He adds that
CSHL has collaborations with many hospitals, notably Memorial Sloan
Kettering Cancer Center and the North Shore-LIJ Health System, to bring
single-cell analysis to the clinic.
For Schatz, Gingko represents a culmination of CSHL's efforts over
the past decade—spearheaded by CSHL Professor Michael Wigler—to pioneer
techniques for studying single cells. "Cold Spring Harbor has
established itself as the world leader in single-cell analysis," says
Schatz. "We've invented many of the technologies and techniques
important to the field and now we've taken all this knowledge and
bundled it up so that researchers around the world can take advantage of
our expertise."
SOURCE;
Medicalxpress and Provided by:
Cold Spring Harbor Laboratory



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