Conclusions: The method is quick and easy to apply, straightforward to interpret, and represents a substantial cost saving compared to single -
cell genome sequencing techniques.
«Multiclonal invasion identified in early breast tumors by topographic single
cell genome sequencing»
Navin's team developed Nuc - Sec as a single -
cell genome sequencing method and applied it to study how cell mutations occur in both types of breast cancer.
Not exact matches
To determine how the
cells switch from one type to another, they took three human uterine carcinosarcoma samples and
sequenced the
genomes of
cells in two parts of each tumor: the carcinoma and sarcoma components.
Lacks» family was never asked for permission to harvest her
cells, an ethical violation made worse in March when German researchers published the
sequence of the HeLa
genome without asking.
The man responsible for one of the original
sequences of the human
genome as well as the team that brought you the first living
cell running on human - made DNA now hopes to harness algae to make everything humanity needs.
«These predictive algorithms seem to do a good job when CRISPR is performed in
cells or tissues in a dish, but whole
genome sequencing has not been employed to look for all off - target effects in living animals,» says co-author Alexander Bassuk, MD, PhD, professor of pediatrics at the University of Iowa.
When researchers
sequenced the sponge's
genome in 2010, they found genes that help individual
cells cooperate as a group: how to divide, send signals to one another, and distinguish between friends and outsiders.
Slight modifications in their
genome sequences play a crucial role in the conversion of pluripotent stem
cells into various differentiated
cell types.
An analysis of the HPV16
genome from 5,570 human
cell and tissue samples revealed that the virus actually consists of thousands of unique
genomes, such that infected women living in the same region often have different HPV16
sequences and variable risks to cancer.
To address this gap in knowledge, Mirabello and Schiffman teamed up with co-senior author Robert Burk of Albert Einstein College of Medicine to
sequence the whole
genomes of 5,570 HPV16 - infected
cell and tissue samples from women around the world and to identify associations between HPV16 genetic variants and the risk of cervical precancer and cancer.
Scientists investigating the earliest stages of cancer development used an exquisitely sensitive
sequencing method capable of detecting DNA mutations present in as few as 1.6 per cent of blood
cells, to analyse 15 locations in the
genome, which are known to be altered in leukemia.
There, some of the added DNA was swapped with the matching target
sequences in the
cells»
genomes.
Sequencing the
genome of one such organism, King and her colleagues found genes that code for pieces of the same proteins used for the binding of
cells and communication between
cells in animals — functions that would be unexpected in such an organism.
«Whole -
genome, single -
cell [
sequencing] costs about the same as bulk -
cell sequencing,» says BGI's Peng.
Researchers can send their
cells to SingulOmics for preparation and
genome amplification, and then have the amplified DNA sent to Novogene for
sequencing.
The diversity of
genome amplification options underscores the importance of having a clear experimental question in mind before starting a single -
cell sequencing project.
For DNA
sequencing, that requires first amplifying each
cell's
genome in order to construct a library for
sequencing.
«Whole -
genome, single -
cell [
sequencing] costs about the same as bulk -
cell sequencing.»
The result was an extremely high - throughput
sequencing protocol that, in a single run, can cover portions of the
genomes of over 50,000 microbial
cells (2).
Though these barcodes are synthesized differently from 10x Genomics» RNA -
sequencing barcodes, their purpose is similar: to link each
cell's amplified
genome pieces to a unique identifying
sequence.
The man who first
sequenced the human
genome and designed the first synthetic
cell explains why simple algae — and some genetic engineering — may hold the key to our future
Cell - free genomic DNA isolated from human
cells was cleaved with preassembled, recombinant Cpf1 RNPs and subjected to whole -
genome sequencing.
Roughly speaking, ChIP
sequencing can be compared to a microscope, which enables us to observe the presence of different
cell components in the entire
genome at a given time.
The six previously known fly rhodopsins account for the full function of photoreceptor
cells in the fly's eyes, so although the fruit fly
genome contained the
sequence of a seventh rhodopsin, the role of Rh7 was unclear.
Current
genome sequencing techniques involve the chemical disintegration of samples of red blood
cells from infected patients to obtain parasite DNA, which are then
sequenced.
«The DNA
sequence itself tells us very little about how
cells actual decodes the DNA, and to understand this we need to map out which
cell components are present in different parts of the
genome at a specific time.
DNA
sequencing is used for mapping the
sequence of the base pairs, which our DNA consists of, and ChIP
sequencing is a derived method in which the
sequences are used to determine the presence of different
cell components in the
genome at a given time.
Not only has the parasitic micro jellyfish evolved a stripped - down body plan of just a few
cells, but via data generated at the KU Medical Center's
Genome Sequencing Facility researchers also found the myxozoan genome was drastically simpl
Genome Sequencing Facility researchers also found the myxozoan
genome was drastically simpl
genome was drastically simplified.
Focusing on DNA from chloroplasts and mitochondria — energy - producing structures in
cells that have their own
genomes — the researchers produced 49,000 genetic
sequences.
The team integrated three, complementary gene
sequencing approaches to look for mutations in tumor
cells from SS patients: whole -
genome sequencing in six subjects,
sequencing of all protein - coding regions (exomes) in 66 subjects, and comparing variation in the number of copies of all genes across the
genome in 80 subjects.
Professor Gianni Liti, a senior author on the paper from the Institute for Research on Cancer and Ageing, Nice, said: «We were able to study the evolution in time by combining
genome sequences of the
cell populations and tracking the growth characteristics of the yeast
cells.
The
genomes of these 377 bacterial isolates, plus an additional 107 single bacterial
cells from roots of A. thaliana, were then
sequenced, assembled, and annotated at the JGI.
«This study demonstrates the potential of combining functional profiling of
cells with the characterizations of cancer
genomes via next generation
sequencing,» said co-senior author Jill P. Mesirov, PhD, professor and associate vice chancellor for computational health sciences at UC San Diego School of Medicine.
In order to locate all gene switches, the Freiburg research team used modern
sequencing methods to examine the entire
genome — DNA, epigenetic markers and RNA — during the development, maturation and disease of human cardiac muscle
cells.
A human
genome contains roughly 3 billion nucleotides in linear
sequence, and that is the same, again to a large approximation, in every
cell type throughout life.
Moreover, as
genomes of other animals are
sequenced, «there will be a lot of biology that will be clarified,» says Tom Pollard, a
cell biologist at Yale University in New Haven, Connecticut.
The study was performed using single stem
cells cultivated to provide sufficient DNA for whole
genome sequencing.
Without the
genome sequence of Lacks» healthy
cells or that of her original tumor, it is difficult to trace the origin of these alterations.
As part of ENCODE, 32 institutions did computer analyses, biochemical tests, and
sequencing studies on 147
cell types — six fairly extensively — to find out what each of the
genome's 3 billion bases does.
To study excision repair in
cells, Sancar, Selby and colleagues recently developed a new technique, XR - seq, which allows investigators to isolate and
sequence the small lengths of adduct - damaged DNA that are snipped from the
genome during the excision repair process.
When researchers
sequenced the chimpanzee
genome in 2005, the biggest difference between it and the human
genome was the extinct PtERV1 retrovirus, which inserted its DNA into the
cells it infected like HIV does today.
Derived mostly from human embryonic kidney 293T (HEK293T) and HeLa
cell lines, EdiGene Knockout (KO) Cell Lysates have been optimized through the use of genome editing technology and validated at the genomic level through PCR and Sanger - sequencing techniques to ensure the accuracy and knockout of the target g
cell lines, EdiGene Knockout (KO)
Cell Lysates have been optimized through the use of genome editing technology and validated at the genomic level through PCR and Sanger - sequencing techniques to ensure the accuracy and knockout of the target g
Cell Lysates have been optimized through the use of
genome editing technology and validated at the genomic level through PCR and Sanger -
sequencing techniques to ensure the accuracy and knockout of the target gene.
After the sorting, we performed whole
genome amplification on individual aggregates then
sequenced the 16S rRNA marker genes to identify
cells comprising the aggregate.
In previous studies, including recent
genome sequencing of cancer patients, human SETD2 has been implicated in several cancer types, especially in renal
cell carcinoma — the most common kind of kidney cancer.
«Scientists
sequence genome of worm that can regrow body parts, seeking stem
cell insights: Worm's
genome could lead to better understanding of its regenerative prowess, advance stem
cell biology.»
The first study to
sequence and analyze the entire
genome of a HeLa
cell line, along with access to its
sequence data, has been published Aug. 7 in its final version, by G3: Genes
Genomes Genetics, an open - access, scientific journal of the Genetics Society of America.
The new controlled access policy for full
genome sequence data from HeLa
cells will give the Lacks family the ability to have a role in work being done with the HeLa
genome sequences and track any resulting discoveries.
Under the policy, biomedical researchers who agree to abide by terms set forth in the HeLa
Genome Data Use Agreement will be able to apply to NIH for access to the full genome sequence data from HeLa
Genome Data Use Agreement will be able to apply to NIH for access to the full
genome sequence data from HeLa
genome sequence data from HeLa
cells.
Dr. Steinmetz and his team found the
genome of the HeLa
cell line that they
sequenced differs dramatically from a normal human
genome sequence.