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MOS, DAC, ect are submods made by other people then the developers and are unofficial, but add extra content. Only registered members can share their thoughts.

Join the community today totally free - or sign in with your social account on the right and join in the conversation. It's hard not to give this one a The only criticisms that i could give: As for right now, it lacks some really important plot parts from the earlier Third Age.

But Sub-Campaigns for each faction or some could definitely help on this subject. We use cookies to enable you to log in, set your site preferences, analyse site traffic, personalise content and provide relevant advertising.

Find out more and change your settings in our privacy policy. Kingdoms mod Released Third Age - Total War 3.

Gondor Faction Preview updated Jan 20 News 6 comments Many Gondorian units were completely reworked and improved. Mordor Faction Preview Released Jan 4 News 4 comments We have released our fifth faction preview, the latest one released is Mordor.

Dwarves Faction Preview Released Jan 4 News 3 comments We have released our fourth faction preview, the latest one released is Dwarves.

Harad Faction Preview Released Jul 25 News 14 comments We have released our third faction preview, the latest one released is Harad.

Click on read more to see the full changelog and notes. Third Age Total War Patch 2. Third Age - Total War 2.

Guest Oct 15 This comment is currently awaiting admin approval, join now to view. SemproniusDensus Oct 2 Why i got crash on startup?

Got installed latest MTWE and still can't start it? Loht Sep 18 Install Divide and Conquer. Works awesome and adds new content to this mod.

Anything i can do? Loht Sep 14 Create a folder named "saves" in your third age mod folder. Sign in or join with: Release date Released Dec 3 by X4VI3R.

Genre Real Time Strategy. Link to Third Age - Total War by selecting a button and using the embed code provided more Rank 36 of 36, Visits 9,, today.

Last Update 9 months ago. You may also like. View All Top Mods. Total War Medieval II: Ancients Total war Medieval II: The high error rates involved with third generation sequencing are inevitably problematic for the purpose of characterizing individual differences that exist between members of the same species.

Genome assembly is the reconstruction of whole genome DNA sequences. This is generally done with two fundamentally different approaches.

When a reference genome is available, as one is in the case of human, newly sequenced reads could simply be aligned to the reference genome in order to characterize its properties.

In addition, reference genomes do not yet exist for most organisms. De novo assembly is the alternative genome assembly approach to reference alignment.

It refers to the reconstruction of whole genome sequences entirely from raw sequence reads. This method would be chosen when there is no reference genome, when the species of the given organism is unknown as in metagenomics , or when there exist genetic variants of interest that may not be detected by reference genome alignment.

Given the short reads produced by the current generation of sequencing technologies, de novo assembly is a major computational problem. It is normally approached by an iterative process of finding and connecting sequence reads with sensible overlaps.

Various computational and statistical techniques, such as de bruijn graphs and overlap layout consensus graphs, have been leveraged to solve this problem.

Nonetheless, due to the highly repetitive nature of eukaryotic genomes, accurate and complete reconstruction of genome sequences in de novo assembly remains challenging.

Pair end reads have been posed as a possible solution, though exact fragment lengths are often unknown and must be approximated.

Long read lengths offered by third generation sequencing may alleviate many of the challenges currently faced by de novo genome assemblies.

For example, if an entire repetitive region can be sequenced unambiguously in a single read, no computation inference would be required.

Computational methods have been proposed to alleviate the issue of high error rates. For example, in one study, it was demonstrated that de novo assembly of a microbial genome using PacBio sequencing alone performed superior to that of second generation sequencing.

Third generation sequencing may also be used in conjunction with second generation sequencing. This approach is often referred to as hybrid sequencing.

For example, long reads from third generation sequencing may be used to resolve ambiguities that exist in genomes previously assembled using second generation sequencing.

On the other hand, short second generation reads have been used to correct errors in that exist in the long third generation reads.

In general, this hybrid approach has been shown to improve de novo genome assemblies significantly. DNA modifications and resulting gene expression can vary across cell types, temporal development, with genetic ancestry, can change due to environmental stimuli and are heritable.

After the discovery of DNAm, researchers have also found its correlation to diseases like cancer and autism.

The current most common methods for examining methylation state require an assay that fragments DNA before standard second generation sequencing on the Illumina platform.

As a result of short read length, information regarding the longer patterns of methylation are lost. Then the trained model was used to detect 5mC in MinION genomic reads from a human cell line which already had a reference methylome.

A straightforward Mann-Whitney U test can detect modified portions of the E. PacBio sequencing has also been used to detect DNA methylation.

In this platform the pulse width - the width of a fluorescent light pulse - corresponds to a specific base. In it was shown that the interpulse distance in control and methylated samples are different, and there is a "signature" pulse width for each methylation type.

Other forms of DNA modifications — from heavy metals, oxidation, or UV damage — are also possible avenues of research using Oxford Nanopore and PacBio third generation sequencing.

Processing of the raw data — such as normalization to the median signal — was needed on MinION raw data, reducing real-time capability of the technology.

MinION has low throughput; since multiple overlapping reads are hard to obtain, this further leads to accuracy problems of downstream DNA modification detection.

Both the hidden Markov model and statistical methods used with MinION raw data require repeated observations of DNA modifications for detection, meaning that individual modified nucleotides need to be consistently present in multiple copies of the genome, e.

For the PacBio platform, too, depending on what methylation you expect to find, coverage needs can vary. As of March , other epigenetic factors like histone modifications have not been discoverable using third-generation technologies.

Longer patterns of methylation are often lost because smaller contigs still need to be assembled. Transcriptomics is the study of the transcriptome , usually by characterizing the relative abundances of messenger RNA molecules the tissue under study.

According to the central dogma of molecular biology , genetic information flows from double stranded DNA molecules to single stranded mRNA molecules where they can be readily translated into function protein molecules.

By studying the transcriptome, one can gain valuable insight into the regulation of gene expressions. While expression levels as the gene level can be more or less accurately depicted by second generation sequencing, transcript level information is still an important challenge.

Third generation sequencing technologies hold promising prospects in resolving this issue by enabling sequencing of mRNA molecules at their full lengths.

Alternative splicing AS is the process by which a single gene may give rise to multiple distinct mRNA transcripts and consequently different protein translations.

Advancing knowledge in this area has critical implications for the study of biology in general. The current generation of sequencing technologies produce only short reads, putting tremendous limitation on the ability to detect distinct transcripts; short reads must be reverse engineered into original transcripts that could have given rise to the resulting read observations.

A study published in surveyed 25 different existing transcript reconstruction protocols. Third generation sequencing technologies have demonstrated promising prospects in solving the problem of transcript detection as well as mRNA abundance estimation at the level of transcripts.

While error rates remain high, third generation sequencing technologies have the capability to produce much longer read lengths.

The trouble with higher error rates may be alleviated by supplementary high quality short reads. This approach has been previously tested and reported to reduce the error rate by more than 3 folds.

Metagenomics is the analysis of genetic material recovered directly from environmental samples. The main advantage for third-generation sequencing technologies in metagenomics is their speed of sequencing in comparison to second generation techniques.

This method would be chosen when there is no reference genome, when the species of the given organism is unknown as in metagenomics , or when there exist genetic variants of interest that may not be detected by reference genome alignment.

Given the short reads produced by the current generation of sequencing technologies, de novo assembly is a major computational problem. It is normally approached by an iterative process of finding and connecting sequence reads with sensible overlaps.

Various computational and statistical techniques, such as de bruijn graphs and overlap layout consensus graphs, have been leveraged to solve this problem.

Nonetheless, due to the highly repetitive nature of eukaryotic genomes, accurate and complete reconstruction of genome sequences in de novo assembly remains challenging.

Pair end reads have been posed as a possible solution, though exact fragment lengths are often unknown and must be approximated.

Long read lengths offered by third generation sequencing may alleviate many of the challenges currently faced by de novo genome assemblies.

For example, if an entire repetitive region can be sequenced unambiguously in a single read, no computation inference would be required.

Computational methods have been proposed to alleviate the issue of high error rates. For example, in one study, it was demonstrated that de novo assembly of a microbial genome using PacBio sequencing alone performed superior to that of second generation sequencing.

Third generation sequencing may also be used in conjunction with second generation sequencing. This approach is often referred to as hybrid sequencing.

For example, long reads from third generation sequencing may be used to resolve ambiguities that exist in genomes previously assembled using second generation sequencing.

On the other hand, short second generation reads have been used to correct errors in that exist in the long third generation reads.

In general, this hybrid approach has been shown to improve de novo genome assemblies significantly. DNA modifications and resulting gene expression can vary across cell types, temporal development, with genetic ancestry, can change due to environmental stimuli and are heritable.

After the discovery of DNAm, researchers have also found its correlation to diseases like cancer and autism. The current most common methods for examining methylation state require an assay that fragments DNA before standard second generation sequencing on the Illumina platform.

As a result of short read length, information regarding the longer patterns of methylation are lost. Then the trained model was used to detect 5mC in MinION genomic reads from a human cell line which already had a reference methylome.

A straightforward Mann-Whitney U test can detect modified portions of the E. PacBio sequencing has also been used to detect DNA methylation. In this platform the pulse width - the width of a fluorescent light pulse - corresponds to a specific base.

In it was shown that the interpulse distance in control and methylated samples are different, and there is a "signature" pulse width for each methylation type.

Other forms of DNA modifications — from heavy metals, oxidation, or UV damage — are also possible avenues of research using Oxford Nanopore and PacBio third generation sequencing.

Processing of the raw data — such as normalization to the median signal — was needed on MinION raw data, reducing real-time capability of the technology.

MinION has low throughput; since multiple overlapping reads are hard to obtain, this further leads to accuracy problems of downstream DNA modification detection.

Both the hidden Markov model and statistical methods used with MinION raw data require repeated observations of DNA modifications for detection, meaning that individual modified nucleotides need to be consistently present in multiple copies of the genome, e.

For the PacBio platform, too, depending on what methylation you expect to find, coverage needs can vary. As of March , other epigenetic factors like histone modifications have not been discoverable using third-generation technologies.

Longer patterns of methylation are often lost because smaller contigs still need to be assembled. Transcriptomics is the study of the transcriptome , usually by characterizing the relative abundances of messenger RNA molecules the tissue under study.

According to the central dogma of molecular biology , genetic information flows from double stranded DNA molecules to single stranded mRNA molecules where they can be readily translated into function protein molecules.

By studying the transcriptome, one can gain valuable insight into the regulation of gene expressions. While expression levels as the gene level can be more or less accurately depicted by second generation sequencing, transcript level information is still an important challenge.

Third generation sequencing technologies hold promising prospects in resolving this issue by enabling sequencing of mRNA molecules at their full lengths.

Alternative splicing AS is the process by which a single gene may give rise to multiple distinct mRNA transcripts and consequently different protein translations.

Advancing knowledge in this area has critical implications for the study of biology in general. The current generation of sequencing technologies produce only short reads, putting tremendous limitation on the ability to detect distinct transcripts; short reads must be reverse engineered into original transcripts that could have given rise to the resulting read observations.

A study published in surveyed 25 different existing transcript reconstruction protocols. Third generation sequencing technologies have demonstrated promising prospects in solving the problem of transcript detection as well as mRNA abundance estimation at the level of transcripts.

While error rates remain high, third generation sequencing technologies have the capability to produce much longer read lengths.

The trouble with higher error rates may be alleviated by supplementary high quality short reads. This approach has been previously tested and reported to reduce the error rate by more than 3 folds.

Metagenomics is the analysis of genetic material recovered directly from environmental samples. The main advantage for third-generation sequencing technologies in metagenomics is their speed of sequencing in comparison to second generation techniques.

Speed of sequencing is important for example in the clinical setting i. Oxford Nanopore's MinION was used in for real-time metagenomic detection of pathogens in complex, high-background clinical samples.

The first Ebola virus EBV read was sequenced 44 seconds after data acquisition. A common phylogenetic marker for microbial community diversity studies is the 16S ribosomal RNA gene.

For the same reason eukaryotic pathogens were not identified. Unique barcodes may allow for more multiplexing.

The per base sequencing cost is still significantly more than that of MiSeq. MOS, DAC, ect are submods made by other people then the developers and are unofficial, but add extra content.

Only registered members can share their thoughts. Join the community today totally free - or sign in with your social account on the right and join in the conversation.

It's hard not to give this one a The only criticisms that i could give: As for right now, it lacks some really important plot parts from the earlier Third Age.

But Sub-Campaigns for each faction or some could definitely help on this subject. We use cookies to enable you to log in, set your site preferences, analyse site traffic, personalise content and provide relevant advertising.

Find out more and change your settings in our privacy policy. Kingdoms mod Released Third Age - Total War 3.

Gondor Faction Preview updated Jan 20 News 6 comments Many Gondorian units were completely reworked and improved. Mordor Faction Preview Released Jan 4 News 4 comments We have released our fifth faction preview, the latest one released is Mordor.

Dwarves Faction Preview Released Jan 4 News 3 comments We have released our fourth faction preview, the latest one released is Dwarves.

Harad Faction Preview Released Jul 25 News 14 comments We have released our third faction preview, the latest one released is Harad.

Click on read more to see the full changelog and notes. Third Age Total War Patch 2. Third Age - Total War 2. Guest Oct 15 This comment is currently awaiting admin approval, join now to view.

SemproniusDensus Oct 2 Why i got crash on startup? Got installed latest MTWE and still can't start it? Loht Sep 18 Install Divide and Conquer.

Works awesome and adds new content to this mod. Anything i can do? Loht Sep 14 Create a folder named "saves" in your third age mod folder.

Sign in or join with: Release date Released Dec 3 by X4VI3R. Genre Real Time Strategy. Link to Third Age - Total War by selecting a button and using the embed code provided more Rank 36 of 36, Visits 9,, today.

Last Update 9 months ago. You may also like. View All Top Mods. Total War Medieval II: Ancients Total war Medieval II:

Third Deutsch Video

Lupin the Third - Der Meisterdieb Filme HD Deutsch

Third deutsch -

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