Frontiers in Microbiology,
Год журнала:
2019,
Номер
9
Опубликована: Янв. 24, 2019
The
improvement
of
sequencing
technologies
has
facilitated
generalization
metagenomic
sequencing,
which
become
a
standard
procedure
for
analyzing
the
structure
and
functionality
microbiomes.
Bioinformatic
analysis
results
poses
challenge
because
it
involves
many
different
complex
steps.
SqueezeMeta
is
fully
automatic
pipeline
metagenomics/metatranscriptomics,
covering
all
steps
analysis.
includes
multi-metagenome
support
that
enables
co-assembly
related
metagenomes
retrieval
individual
genomes
via
binning
procedures.
features
several
unique
characteristics:
or
unlimited
number
merging
assembled
metagenomes,
both
with
read
mapping
estimation
abundances
genes
in
each
metagenome.
It
also
bin
checking
retrieving
genomes.
Internal
checks
assembly
provide
information
about
consistency
contigs
bins.
Moreover,
are
stored
MySQL
database,
where
they
can
be
easily
exported
shared,
inspected
anywhere
using
flexible
web
interface
allows
simple
creation
queries.
We
illustrate
potential
by
32
gut
way,
enabling
million
hundreds
genomic
One
motivations
development
was
producing
software
capable
running
small
desktop
computers
thus
amenable
to
users
settings.
were
able
co-assemble
two
these
complete
full
less
than
one
day
laptop
computer.
This
reveals
capacity
run
without
high-performance
computing
infrastructure
absence
any
network
connectivity.
therefore
adequate
situ,
real
time
produced
nanopore
sequencing.
downloaded
from
https://github.com/jtamames/SqueezeMeta.
Molecular Biology and Evolution,
Год журнала:
2021,
Номер
38(10), С. 4647 - 4654
Опубликована: Июль 25, 2021
Abstract
Methods
for
evaluating
the
quality
of
genomic
and
metagenomic
data
are
essential
to
aid
genome
assembly
procedures
correctly
interpret
results
subsequent
analyses.
BUSCO
estimates
completeness
redundancy
processed
based
on
universal
single-copy
orthologs.
Here,
we
present
new
functionalities
major
improvements
software,
as
well
renewal
expansion
underlying
sets
in
sync
with
OrthoDB
v10
release.
Among
novelties,
now
enables
phylogenetic
placement
input
sequence
automatically
select
most
appropriate
set
assessment,
allowing
analysis
metagenome-assembled
genomes
unknown
origin.
A
newly
introduced
workflow
increases
efficiency
runtimes
especially
large
eukaryotic
genomes.
is
only
tool
capable
assessing
both
prokaryotic
species,
can
be
applied
various
types,
from
assemblies
bins,
transcriptomes
gene
sets.
Nature Biotechnology,
Год журнала:
2017,
Номер
35(8), С. 725 - 731
Опубликована: Авг. 1, 2017
We
present
two
standards
developed
by
the
Genomic
Standards
Consortium
(GSC)
for
reporting
bacterial
and
archaeal
genome
sequences.
Both
are
extensions
of
Minimum
Information
about
Any
(x)
Sequence
(MIxS).
The
a
Single
Amplified
Genome
(MISAG)
Metagenome-Assembled
(MIMAG),
including,
but
not
limited
to,
assembly
quality,
estimates
completeness
contamination.
These
can
be
used
in
combination
with
other
GSC
checklists,
including
(MIGS),
Metagenomic
(MIMS),
Marker
Gene
(MIMARKS).
Community-wide
adoption
MISAG
MIMAG
will
facilitate
more
robust
comparative
genomic
analyses
diversity.
Nature Microbiology,
Год журнала:
2017,
Номер
2(11), С. 1533 - 1542
Опубликована: Сен. 11, 2017
Abstract
Challenges
in
cultivating
microorganisms
have
limited
the
phylogenetic
diversity
of
currently
available
microbial
genomes.
This
is
being
addressed
by
advances
sequencing
throughput
and
computational
techniques
that
allow
for
cultivation-independent
recovery
genomes
from
metagenomes.
Here,
we
report
reconstruction
7,903
bacterial
archaeal
>1,500
public
All
are
estimated
to
be
≥50%
complete
nearly
half
≥90%
with
≤5%
contamination.
These
increase
genome
trees
>30%
provide
first
representatives
17
three
candidate
phyla.
We
also
recovered
245
Patescibacteria
superphylum
(also
known
as
Candidate
Phyla
Radiation)
find
relative
this
group
varies
substantially
different
protein
marker
sets.
The
scale
quality
data
set
demonstrate
recovering
metagenomes
provides
an
expedient
path
forward
exploring
dark
matter.
G3 Genes Genomes Genetics,
Год журнала:
2020,
Номер
10(4), С. 1361 - 1374
Опубликована: Фев. 19, 2020
Reconstruction
of
target
genomes
from
sequence
data
produced
by
instruments
that
are
agnostic
as
to
the
species-of-origin
may
be
confounded
contaminant
DNA.
Whether
introduced
during
sample
processing
or
through
co-extraction
alongside
DNA,
if
insufficient
care
is
taken
assembly
process,
final
assembled
genome
a
mixture
several
species.
Such
assemblies
can
confound
sequence-based
biological
inference
and,
when
deposited
in
public
databases,
included
downstream
analyses
users
unaware
underlying
problems.
We
present
BlobToolKit,
software
suite
aid
researchers
identifying
and
isolating
non-target
draft
publicly
available
assemblies.
BlobToolKit
used
process
assembly,
read
analysis
files
for
fully
reproducible
interactive
exploration
browser-based
Viewer.
filter
helping
produce
with
high
credibility.
have
been
running
an
automated
pipeline
on
eukaryotic
International
Nucleotide
Sequence
Data
Collaboration
making
results
instance
Viewer
at
https://blobtoolkit.genomehubs.org/view
aim
complete
all
then
maintain
currency
flow
new
genomes.
worked
embed
these
views
into
presentation
European
Archive,
providing
indication
quality
record
links
out
allow
full
Cell,
Год журнала:
2019,
Номер
176(3), С. 649 - 662.e20
Опубликована: Янв. 1, 2019
The
body-wide
human
microbiome
plays
a
role
in
health,
but
its
full
diversity
remains
uncharacterized,
particularly
outside
of
the
gut
and
international
populations.
We
leveraged
9,428
metagenomes
to
reconstruct
154,723
microbial
genomes
(45%
high
quality)
spanning
body
sites,
ages,
countries,
lifestyles.
recapitulated
4,930
species-level
genome
bins
(SGBs),
77%
without
public
repositories
(unknown
SGBs
[uSGBs]).
uSGBs
are
prevalent
(in
93%
well-assembled
samples),
expand
underrepresented
phyla,
enriched
non-Westernized
populations
(40%
total
SGBs).
annotated
2.85
M
genes
SGBs,
many
associated
with
conditions
including
infant
development
(94,000)
or
Westernization
(106,000).
permit
deeper
analyses
increase
average
mappability
metagenomic
reads
from
67.76%
87.51%
(median
94.26%)
65.14%
82.34%
mouth.
thus
identify
thousands
yet-to-be-named
species,
pangenomes
human-associated
microbes,
allow
better
exploitation
technologies.
Abstract
Genome
sequence
assemblies
provide
the
basis
for
our
understanding
of
biology.
Generating
error-free
is
therefore
ultimate,
but
sadly
still
unachieved
goal
a
multitude
research
projects.
Despite
ever-advancing
improvements
in
data
generation,
assembly
algorithms
and
pipelines,
no
automated
approach
has
so
far
reliably
generated
near
genome
eukaryotes.
Whilst
working
towards
improved
datasets
fully
evaluation
curation
actively
used
to
bridge
this
shortcoming
significantly
reduce
number
errors.
In
addition
increase
product
value,
insights
gained
from
are
fed
back
into
strategy
contribute
notable
quality.
We
describe
tried
tested
using
gEVAL,
browser.
outline
procedures
applied
gEVAL
also
recommendations
gEVAL-independent
context
facilitate
uptake
wider
community.
Nature Communications,
Год журнала:
2016,
Номер
7(1)
Опубликована: Окт. 24, 2016
Abstract
The
subterranean
world
hosts
up
to
one-fifth
of
all
biomass,
including
microbial
communities
that
drive
transformations
central
Earth’s
biogeochemical
cycles.
However,
little
is
known
about
how
complex
in
such
environments
are
structured,
and
inter-organism
interactions
shape
ecosystem
function.
Here
we
apply
terabase-scale
cultivation-independent
metagenomics
aquifer
sediments
groundwater,
reconstruct
2,540
draft-quality,
near-complete
complete
strain-resolved
genomes
represent
the
majority
bacterial
phyla
as
well
47
newly
discovered
phylum-level
lineages.
Metabolic
analyses
spanning
this
vast
phylogenetic
diversity
representing
36%
organisms
detected
system
used
document
distribution
pathways
coexisting
organisms.
Consistent
with
prior
findings
indicating
metabolic
handoffs
simple
consortia,
find
few
within
community
can
conduct
multiple
sequential
redox
transformations.
As
environmental
conditions
change,
different
assemblages
selected
for,
altering
linkages
among
major